Canonical Allele Identifier: CA14526648
Gene: ENOSF1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2612101

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.676473C>T , CM000680.2:g.676473C>T GRCh38
NC_000018.9:g.676473C>T , CM000680.1:g.676473C>T GRCh37
NC_000018.8:g.666473C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001126123.3:c.902+872G>A VV NP_001119595.1:p.=
NM_017512.5:c.1148+872G>A VV NP_059982.2:p.=
NM_202758.3:c.1169+872G>A VV NP_974487.1:p.=
XM_005258118.2:c.605+872G>A XP_005258175.1:p.=
XM_011525677.1:c.1190+872G>A XP_011523979.1:p.=
XM_011525678.1:c.1181+872G>A XP_011523980.1:p.=
XM_011525679.1:c.1175+872G>A XP_011523981.1:p.=
XM_011525680.1:c.1163+872G>A XP_011523982.1:p.=
XM_011525681.1:c.1151+872G>A XP_011523983.1:p.=
XM_011525682.1:c.1124+872G>A XP_011523984.1:p.=
XM_011525683.1:c.1001+872G>A XP_011523985.1:p.=
XM_011525684.1:c.974+872G>A XP_011523986.1:p.=
XM_011525685.1:c.962+872G>A XP_011523987.1:p.=
XM_011525686.1:c.938+872G>A XP_011523988.1:p.=
XM_011525687.1:c.920+872G>A XP_011523989.1:p.=
XM_011525688.1:c.917+872G>A XP_011523990.1:p.=
XM_011525689.1:c.785+872G>A XP_011523991.1:p.=
XM_011525690.1:c.785+872G>A XP_011523992.1:p.=
XM_011525691.1:c.731+872G>A XP_011523993.1:p.=
XM_011525692.1:c.731+872G>A XP_011523994.1:p.=
XM_011525693.1:c.731+872G>A XP_011523995.1:p.=
XM_011525694.1:c.716+872G>A XP_011523996.1:p.=
XM_011525695.1:c.692+872G>A XP_011523997.1:p.=
XM_011525696.1:c.620+872G>A XP_011523998.1:p.=
XM_011525697.1:c.578+872G>A XP_011523999.1:p.=
XM_011525698.1:c.578+872G>A XP_011524000.1:p.=
XM_011525699.1:c.578+872G>A XP_011524001.1:p.=
XR_243810.3:n.1184+872G>A
XR_243811.2:n.1209+872G>A
XR_430041.2:n.1304+872G>A
XR_935066.1:n.1069+872G>A
XR_935067.1:n.928-1071G>A
NM_001318760.1:c.605+872G>A VV NP_001305689.1:p.=
NM_001354065.1:c.902+872G>A VV NP_001340994.1:p.=
NM_001354066.1:c.1106+872G>A VV NP_001340995.1:p.=
NM_001354067.1:c.1292+872G>A VV NP_001340996.1:p.=
NM_001354068.1:c.1061+872G>A VV NP_001340997.1:p.=
NM_017512.6:c.1148+872G>A VV NP_059982.2:p.=
NM_202758.4:c.1250+872G>A VV NP_974487.2:p.=
NR_148706.1:n.1109+872G>A
NR_148707.1:n.1225+872G>A
NR_148708.1:n.1473+872G>A
NR_148709.1:n.1159+872G>A
NR_148710.1:n.1185+872G>A
NR_148711.1:n.1036+872G>A
NR_148712.1:n.1369+872G>A
XM_017025837.1:c.563+872G>A XP_016881326.1:p.=
XM_024451200.1:c.1169+872G>A XP_024306968.1:p.=
XM_024451201.1:c.1163+872G>A XP_024306969.1:p.=
XM_024451202.1:c.1154+872G>A XP_024306970.1:p.=
XM_024451203.1:c.1124+872G>A XP_024306971.1:p.=
XM_024451204.1:c.1004+872G>A XP_024306972.1:p.=
XM_024451205.1:c.980+872G>A XP_024306973.1:p.=
XM_024451206.1:c.974+872G>A XP_024306974.1:p.=
XM_024451207.1:c.938+872G>A XP_024306975.1:p.=
XM_024451208.1:c.923+872G>A XP_024306976.1:p.=
XM_024451209.1:c.920+872G>A XP_024306977.1:p.=
XM_024451210.1:c.917+872G>A XP_024306978.1:p.=
XM_024451211.1:c.878+872G>A XP_024306979.1:p.=
XM_024451212.1:c.785+872G>A XP_024306980.1:p.=
XM_024451213.1:c.785+872G>A XP_024306981.1:p.=
XM_024451214.1:c.746+872G>A XP_024306982.1:p.=
XM_024451215.1:c.731+872G>A XP_024306983.1:p.=
XM_024451216.1:c.731+872G>A XP_024306984.1:p.=
XM_024451217.1:c.620+872G>A XP_024306985.1:p.=
XM_024451218.1:c.578+872G>A XP_024306986.1:p.=
XM_024451219.1:c.578+872G>A XP_024306987.1:p.=
XM_024451220.1:c.578+872G>A XP_024306988.1:p.=
XR_002958180.1:n.938-1071G>A
XR_430041.4:n.1323+872G>A
NM_017512.7:c.1148+872G>A VV MANE Preferred NP_059982.2:p.=
ENST00000251101.11:c.1148+872G>A ENSP00000251101.7:p.=
ENST00000340116.11:c.1169+872G>A ENSP00000345974.7:p.=
ENST00000383578.7:c.902+872G>A ENSP00000373072.3:p.=
ENST00000580982.5:c.920+872G>A ENSP00000463425.1:p.=
ENST00000581475.5:c.*535+872G>A ENSP00000464614.1:p.=
ENST00000581928.5:n.136-1071G>A
ENST00000582745.5:n.646+872G>A
ENST00000583973.5:n.1729+872G>A
ENST00000584259.6:n.3259+872G>A
ENST00000584453.5:c.*535+872G>A ENSP00000463448.1:p.=
ENST00000584646.5:n.264+872G>A
ENST00000585128.6:n.968+872G>A