Canonical Allele Identifier: CA2577062568
Gene: SULT1C4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108378262_108378263insA , CM000664.2:g.108378262_108378263insA GRCh38
NC_000002.11:g.108994718_108994719insA , CM000664.1:g.108994718_108994719insA GRCh37
NC_000002.10:g.108361150_108361151insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272452.7:c.-76_-75insA MANE Select ENSP00000272452.2:n.-76_-75insA
ENST00000272452.6:c.-76_-75insA ENSP00000272452.2:n.-76_-75insA
ENST00000409309.3:c.-76_-75insA ENSP00000387225.3:n.-76_-75insA
ENST00000494122.1:n.352_353insA
NM_006588.2:c.-76_-75insA NP_006579.2:n.-76_-75insA
XM_005263919.2:c.-76_-75insA XP_005263976.1:n.-76_-75insA
NM_001321770.1:c.-76_-75insA NP_001308699.1:n.-76_-75insA
NM_006588.3:c.-76_-75insA NP_006579.2:n.-76_-75insA
NR_135776.1:n.352_353insA
NR_135779.1:n.352_353insA
NM_006588.4:c.-76_-75insA MANE Select NP_006579.2:n.-76_-75insA
NM_001321770.2:c.-76_-75insA NP_001308699.1:n.-76_-75insA
NR_135776.2:n.309_310insA
NR_135779.2:n.309_310insA