Canonical Allele Identifier: CA2660580161

Gene: SULT1C4

Linked Data

• gnomAD v4: 2-108387199-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108387199T>C , CM000664.2:g.108387199T>C	GRCh38
NC_000002.11:g.109003655T>C , CM000664.1:g.109003655T>C	GRCh37
NC_000002.10:g.108370087T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272452.7:c.797-121T>C MANE Select	ENSP00000272452.2:n.797-121T>C
ENST00000272452.6:c.797-121T>C	ENSP00000272452.2:n.797-121T>C
ENST00000409309.3:c.572-121T>C	ENSP00000387225.3:n.572-121T>C
NM_006588.2:c.797-121T>C	NP_006579.2:n.797-121T>C
XM_005263919.2:c.572-121T>C	XP_005263976.1:n.572-121T>C
NM_001321770.1:c.572-121T>C	NP_001308699.1:n.572-121T>C
NM_006588.3:c.797-121T>C	NP_006579.2:n.797-121T>C
NR_135776.1:n.1049-121T>C
NR_135779.1:n.778-121T>C
XM_017003807.1:c.527-121T>C	XP_016859296.1:n.527-121T>C
NM_006588.4:c.797-121T>C MANE Select	NP_006579.2:n.797-121T>C
NM_001321770.2:c.572-121T>C	NP_001308699.1:n.572-121T>C
NR_135776.2:n.1006-121T>C
NR_135779.2:n.735-121T>C