Canonical Allele Identifier: CA2616340671

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029408-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029408C>A , CM000673.2:g.119029408C>A	GRCh38
NC_000011.9:g.118900118C>A , CM000673.1:g.118900118C>A	GRCh37
NC_000011.8:g.118405328C>A	NCBI36
NG_013331.1:g.6499G>T , LRG_187:g.6499G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.191G>T
ENST00000697846.1:n.191G>T
ENST00000697847.1:n.191G>T
ENST00000697848.1:n.191G>T
ENST00000697849.1:n.435G>T
ENST00000697850.1:n.191G>T
ENST00000697851.1:n.435G>T
ENST00000638186.1:n.265G>T
ENST00000638360.1:n.199G>T
ENST00000638925.1:n.198G>T
ENST00000650539.1:n.367G>T
ENST00000330775.9:c.-39G>T	ENSP00000476242.2:n.-39G>T
ENST00000357590.9:c.-39G>T	ENSP00000476176.2:n.-39G>T
ENST00000525039.5:n.385G>T
ENST00000525102.5:n.719G>T
ENST00000525787.1:n.257G>T
ENST00000526626.6:n.157G>T
ENST00000527992.5:n.189G>T
ENST00000530407.5:n.181G>T
ENST00000532085.1:n.1456G>T
ENST00000532888.6:n.157G>T
ENST00000534384.1:n.182G>T
ENST00000538950.5:c.-188G>T	ENSP00000475991.2:n.-188G>T
ENST00000545985.5:c.-39G>T	ENSP00000475241.2:n.-39G>T
NM_001164277.1:c.-39G>T , LRG_187t1:c.-39G>T	NP_001157749.1:n.-39G>T
NM_001164278.1:c.-39G>T	NP_001157750.1:n.-39G>T
NM_001164279.1:c.-188G>T	NP_001157751.1:n.-188G>T
NM_001164280.1:c.-39G>T	NP_001157752.1:n.-39G>T
NM_001467.5:c.-39G>T	NP_001458.1:n.-39G>T
NM_001164278.2:c.-39G>T	NP_001157750.1:n.-39G>T
NM_001164279.2:c.-188G>T	NP_001157751.1:n.-188G>T
NM_001164280.2:c.-39G>T	NP_001157752.1:n.-39G>T
NM_001467.6:c.-39G>T	NP_001458.1:n.-39G>T
NM_001164277.2:c.-39G>T MANE Select	NP_001157749.1:n.-39G>T