Canonical Allele Identifier: CA382897074

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896675A>T (hg19) ; chr11:g.119025965A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025965A>T , CM000673.2:g.119025965A>T	GRCh38
NC_000011.9:g.118896675A>T , CM000673.1:g.118896675A>T	GRCh37
NC_000011.8:g.118401885A>T	NCBI36
NG_013331.1:g.9941T>A , LRG_187:g.9941T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1128+2T>A
ENST00000697845.1:n.1910T>A
ENST00000697846.1:n.1128+2T>A
ENST00000697847.1:n.1202-208T>A
ENST00000697848.1:n.1214+2T>A
ENST00000697849.1:n.3025T>A
ENST00000697850.1:n.1216T>A
ENST00000697851.1:n.2822+2T>A
ENST00000638186.1:n.1288+2T>A
ENST00000638360.1:n.1120+2T>A
ENST00000638925.1:n.1253+2T>A
ENST00000650539.1:n.1390+2T>A
ENST00000330775.9:c.984+2T>A	ENSP00000476242.2:n.984+2T>A
ENST00000357590.9:c.984+2T>A	ENSP00000476176.2:n.984+2T>A
ENST00000524428.5:n.1220+2T>A
ENST00000525039.5:n.1408+2T>A
ENST00000525102.5:n.1742+2T>A
ENST00000525372.5:n.1082+2T>A
ENST00000526275.5:n.1766+2T>A
ENST00000527992.5:n.1212+2T>A
ENST00000529510.5:n.672+2T>A
ENST00000530407.5:n.1134+2T>A
ENST00000532085.1:n.4367T>A
ENST00000538950.5:c.765+2T>A	ENSP00000475991.2:n.765+2T>A
ENST00000545985.5:c.984+2T>A	ENSP00000475241.2:n.984+2T>A
NM_001164277.1:c.984+2T>A , LRG_187t1:c.984+2T>A	NP_001157749.1:n.984+2T>A
NM_001164278.1:c.984+2T>A	NP_001157750.1:n.984+2T>A
NM_001164279.1:c.765+2T>A	NP_001157751.1:n.765+2T>A
NM_001164280.1:c.984+2T>A	NP_001157752.1:n.984+2T>A
NM_001467.5:c.984+2T>A	NP_001458.1:n.984+2T>A
NM_001164278.2:c.984+2T>A	NP_001157750.1:n.984+2T>A
NM_001164279.2:c.765+2T>A	NP_001157751.1:n.765+2T>A
NM_001164280.2:c.984+2T>A	NP_001157752.1:n.984+2T>A
NM_001467.6:c.984+2T>A	NP_001458.1:n.984+2T>A
NM_001164277.2:c.984+2T>A MANE Select	NP_001157749.1:n.984+2T>A