Canonical Allele Identifier: CA104793057
Gene: BLTP1 HGNC NCBI

Linked Data

dbSNP Id: rs13119723

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122297158A>G , CM000666.2:g.122297158A>G GRCh38
NC_000004.11:g.123218313A>G , CM000666.1:g.123218313A>G GRCh37
NC_000004.10:g.123437763A>G NCBI36
NG_015813.1:g.131556A>G
NG_015813.2:g.131556A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388738.8:c.9338-4142A>G ENSP00000373390.4:n.9338-4142A>G
ENST00000684987.1:n.13464-4142A>G
ENST00000686093.1:c.1341-4142A>G ENSP00000509672.1:n.1341-4142A>G
ENST00000688248.1:c.454-4142A>G
ENST00000690536.1:n.9661-4142A>G
ENST00000693334.1:n.9661-4142A>G
ENST00000693420.1:c.9338-4142A>G ENSP00000509435.1:n.9338-4142A>G
ENST00000679879.1:c.9389-4142A>G MANE Select ENSP00000505357.1:n.9389-4142A>G
ENST00000264501.8:c.9389-4142A>G ENSP00000264501.4:n.9389-4142A>G
ENST00000388738.7:c.9389-4142A>G ENSP00000373390.3:n.9389-4142A>G
ENST00000419325.5:c.3261-4142A>G
NM_015312.3:c.9389-4142A>G NP_056127.2:n.9389-4142A>G
XM_005263282.1:c.9389-4142A>G XP_005263339.1:n.9389-4142A>G
XM_005263287.1:c.9389-4142A>G XP_005263344.1:n.9389-4142A>G
XM_006714343.1:c.9389-4142A>G XP_006714406.1:n.9389-4142A>G
XM_006714344.1:c.9386-4142A>G XP_006714407.1:n.9386-4142A>G
XM_011532319.1:c.9389-4142A>G XP_011530621.1:n.9389-4142A>G
XM_011532320.1:c.9389-4142A>G XP_011530622.1:n.9389-4142A>G
XM_011532321.1:c.9389-4142A>G XP_011530623.1:n.9389-4142A>G
XM_011532322.1:c.9386-4142A>G XP_011530624.1:n.9386-4142A>G
XM_011532323.1:c.9338-4142A>G XP_011530625.1:n.9338-4142A>G
XM_011532324.1:c.9389-4142A>G XP_011530626.1:n.9389-4142A>G
XM_011532325.1:c.9389-4142A>G XP_011530627.1:n.9389-4142A>G
XM_011532326.1:c.9260-4142A>G XP_011530628.1:n.9260-4142A>G
XM_011532327.1:c.9239-4142A>G XP_011530629.1:n.9239-4142A>G
XM_011532328.1:c.9389-4142A>G XP_011530630.1:n.9389-4142A>G
XM_011532329.1:c.9389-4142A>G XP_011530631.1:n.9389-4142A>G
XM_011532330.1:c.7640-4142A>G XP_011530632.1:n.7640-4142A>G
XM_011532331.1:c.9389-4142A>G XP_011530633.1:n.9389-4142A>G
XR_938781.1:n.9762-4142A>G
XR_938782.1:n.9762-4142A>G
XR_938783.1:n.9762-4142A>G
XM_011532320.3:c.9389-4142A>G XP_011530622.1:n.9389-4142A>G
XM_011532321.2:c.9389-4142A>G XP_011530623.1:n.9389-4142A>G
XM_017008695.1:c.9389-4142A>G XP_016864184.1:n.9389-4142A>G
XM_017008696.1:c.9338-4142A>G XP_016864185.1:n.9338-4142A>G
XM_017008697.1:c.9389-4142A>G XP_016864186.1:n.9389-4142A>G
XM_017008698.1:c.6620-4142A>G XP_016864187.1:n.6620-4142A>G
XM_024454243.1:c.7541-4142A>G XP_024310011.1:n.7541-4142A>G
XR_001741335.2:n.9762-4142A>G
XR_001741336.1:n.9762-4142A>G
NM_001384125.1:c.9389-4142A>G MANE Select NP_001371054.1:n.9389-4142A>G
NM_015312.4:c.9389-4142A>G NP_056127.2:n.9389-4142A>G