Canonical Allele Identifier: CA397148067
Community Standard Title: NM_001243279.3(ACSF3):c.1401G>A (p.Trp467Ter)
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89145301G>A , CM000678.2:g.89145301G>A GRCh38
NC_000016.9:g.89211709G>A , CM000678.1:g.89211709G>A GRCh37
NC_000016.8:g.87739210G>A NCBI36
NG_031961.1:g.56493G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001243279.3:c.1401G>A MANE Select NP_001230208.1:p.Trp467Ter
ENST00000614302.5:c.1401G>A MANE Select ENSP00000479130.1:p.Trp467Ter
NM_001127214.3:c.1401G>A NP_001120686.1:p.Trp467Ter
NM_001127214.4:c.1401G>A NP_001120686.1:p.Trp467Ter
NM_001243279.2:c.1401G>A NP_001230208.1:p.Trp467Ter
NM_001284316.1:c.606G>A NP_001271245.1:p.Trp202Ter
NM_001284316.2:c.606G>A NP_001271245.1:p.Trp202Ter
NM_174917.4:c.1401G>A NP_777577.2:p.Trp467Ter
NM_174917.5:c.1401G>A NP_777577.2:p.Trp467Ter
NR_045667.2:n.527G>A
NR_104293.1:n.1835G>A
NR_104293.2:n.1792G>A
NR_147928.1:n.1879G>A
NR_147928.2:n.1836G>A
NR_147929.1:n.1633G>A
NR_147929.2:n.1590G>A
ENST00000317447.8:c.1401G>A ENSP00000320646.4:p.Trp467Ter
ENST00000317447.9:c.1401G>A ENSP00000320646.4:p.Trp467Ter
ENST00000378345.8:c.606G>A ENSP00000367596.4:p.Trp202Ter
ENST00000406948.7:c.1401G>A ENSP00000384627.3:p.Trp467Ter
ENST00000537116.5:n.527G>A
ENST00000537155.1:n.141G>A
ENST00000542688.5:c.*145G>A ENSP00000446281.1:n.*145G>A
ENST00000544543.5:c.606G>A ENSP00000442781.1:p.Trp202Ter
ENST00000562204.1:n.374G>A
ENST00000614302.4:c.1401G>A ENSP00000479130.1:p.Trp467Ter
ENST00000649953.1:c.1611G>A ENSP00000497456.1:p.Trp537Ter
XM_005256293.1:c.1401G>A XP_005256350.1:p.Trp467Ter
XM_005256293.2:c.1401G>A XP_005256350.1:p.Trp467Ter
XM_011522942.1:c.1401G>A XP_011521244.1:p.Trp467Ter
XM_011522943.1:c.1401G>A XP_011521245.1:p.Trp467Ter
XM_017023018.1:c.1401G>A XP_016878507.1:p.Trp467Ter
XM_017023019.1:c.1401G>A XP_016878508.1:p.Trp467Ter
XM_017023020.2:c.-3704G>A XP_016878509.1:n.-3704G>A
XM_017023022.1:c.534G>A XP_016878511.1:p.Trp178Ter
XM_024450186.1:c.606G>A XP_024305954.1:p.Trp202Ter
XM_024450187.1:c.606G>A XP_024305955.1:p.Trp202Ter
XR_001751864.2:n.1648G>A
XR_001751865.1:n.1595G>A
XR_933239.1:n.1842G>A
XR_933240.1:n.1839G>A
XR_933240.3:n.1838G>A
XR_933241.1:n.1596G>A