Canonical Allele Identifier: CA2616340683

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029427-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029427C>A , CM000673.2:g.119029427C>A	GRCh38
NC_000011.9:g.118900137C>A , CM000673.1:g.118900137C>A	GRCh37
NC_000011.8:g.118405347C>A	NCBI36
NG_013331.1:g.6480G>T , LRG_187:g.6480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.172G>T
ENST00000697846.1:n.172G>T
ENST00000697847.1:n.172G>T
ENST00000697848.1:n.172G>T
ENST00000697849.1:n.416G>T
ENST00000697850.1:n.172G>T
ENST00000697851.1:n.416G>T
ENST00000638186.1:n.246G>T
ENST00000638360.1:n.180G>T
ENST00000638925.1:n.179G>T
ENST00000650539.1:n.348G>T
ENST00000330775.9:c.-58G>T	ENSP00000476242.2:n.-58G>T
ENST00000357590.9:c.-58G>T	ENSP00000476176.2:n.-58G>T
ENST00000525039.5:n.366G>T
ENST00000525102.5:n.700G>T
ENST00000525787.1:n.238G>T
ENST00000526626.6:n.138G>T
ENST00000527992.5:n.170G>T
ENST00000530407.5:n.162G>T
ENST00000532085.1:n.1437G>T
ENST00000532888.6:n.138G>T
ENST00000534384.1:n.163G>T
ENST00000538950.5:c.-207G>T	ENSP00000475991.2:n.-207G>T
ENST00000545985.5:c.-58G>T	ENSP00000475241.2:n.-58G>T
NM_001164277.1:c.-58G>T , LRG_187t1:c.-58G>T	NP_001157749.1:n.-58G>T
NM_001164278.1:c.-58G>T	NP_001157750.1:n.-58G>T
NM_001164279.1:c.-207G>T	NP_001157751.1:n.-207G>T
NM_001164280.1:c.-58G>T	NP_001157752.1:n.-58G>T
NM_001467.5:c.-58G>T	NP_001458.1:n.-58G>T
NM_001164278.2:c.-58G>T	NP_001157750.1:n.-58G>T
NM_001164279.2:c.-207G>T	NP_001157751.1:n.-207G>T
NM_001164280.2:c.-58G>T	NP_001157752.1:n.-58G>T
NM_001467.6:c.-58G>T	NP_001458.1:n.-58G>T
NM_001164277.2:c.-58G>T MANE Select	NP_001157749.1:n.-58G>T