Canonical Allele Identifier: CA2616339928

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119025861-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025861G>A , CM000673.2:g.119025861G>A	GRCh38
NC_000011.9:g.118896571G>A , CM000673.1:g.118896571G>A	GRCh37
NC_000011.8:g.118401781G>A	NCBI36
NG_013331.1:g.10045C>T , LRG_187:g.10045C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1129-104C>T
ENST00000697845.1:n.2014C>T
ENST00000697846.1:n.1129-104C>T
ENST00000697847.1:n.1202-104C>T
ENST00000697848.1:n.1215-104C>T
ENST00000697849.1:n.3129C>T
ENST00000697850.1:n.1320C>T
ENST00000697851.1:n.2822+106C>T
ENST00000638186.1:n.1288+106C>T
ENST00000638360.1:n.1120+106C>T
ENST00000638925.1:n.1253+106C>T
ENST00000650539.1:n.1391-104C>T
ENST00000330775.9:c.984+106C>T	ENSP00000476242.2:n.984+106C>T
ENST00000357590.9:c.985-104C>T	ENSP00000476176.2:n.985-104C>T
ENST00000524428.5:n.1220+106C>T
ENST00000525039.5:n.1409-104C>T
ENST00000525102.5:n.1742+106C>T
ENST00000525372.5:n.1082+106C>T
ENST00000526275.5:n.1766+106C>T
ENST00000527992.5:n.1212+106C>T
ENST00000529510.5:n.672+106C>T
ENST00000530407.5:n.1134+106C>T
ENST00000532085.1:n.4471C>T
ENST00000538950.5:c.765+106C>T	ENSP00000475991.2:n.765+106C>T
ENST00000545985.5:c.984+106C>T	ENSP00000475241.2:n.984+106C>T
NM_001164277.1:c.984+106C>T , LRG_187t1:c.984+106C>T	NP_001157749.1:n.984+106C>T
NM_001164278.1:c.985-104C>T	NP_001157750.1:n.985-104C>T
NM_001164279.1:c.765+106C>T	NP_001157751.1:n.765+106C>T
NM_001164280.1:c.984+106C>T	NP_001157752.1:n.984+106C>T
NM_001467.5:c.984+106C>T	NP_001458.1:n.984+106C>T
NM_001164278.2:c.985-104C>T	NP_001157750.1:n.985-104C>T
NM_001164279.2:c.765+106C>T	NP_001157751.1:n.765+106C>T
NM_001164280.2:c.984+106C>T	NP_001157752.1:n.984+106C>T
NM_001467.6:c.984+106C>T	NP_001458.1:n.984+106C>T
NM_001164277.2:c.984+106C>T MANE Select	NP_001157749.1:n.984+106C>T