Canonical Allele Identifier: CA382908593

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118900006T>G (hg19) ; chr11:g.119029296T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029296T>G , CM000673.2:g.119029296T>G	GRCh38
NC_000011.9:g.118900006T>G , CM000673.1:g.118900006T>G	GRCh37
NC_000011.8:g.118405216T>G	NCBI36
NG_013331.1:g.6611A>C , LRG_187:g.6611A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.303A>C
ENST00000697846.1:n.303A>C
ENST00000697847.1:n.303A>C
ENST00000697848.1:n.303A>C
ENST00000697849.1:n.547A>C
ENST00000697850.1:n.303A>C
ENST00000697851.1:n.547A>C
ENST00000638186.1:n.377A>C
ENST00000638360.1:n.311A>C
ENST00000638925.1:n.310A>C
ENST00000650539.1:n.479A>C
ENST00000330775.9:c.74A>C	ENSP00000476242.2:p.Tyr25Ser
ENST00000357590.9:c.74A>C	ENSP00000476176.2:p.Tyr25Ser
ENST00000524428.5:n.74A>C
ENST00000525039.5:n.497A>C
ENST00000525102.5:n.831A>C
ENST00000525372.5:n.74A>C
ENST00000525787.1:n.369A>C
ENST00000526626.6:n.269A>C
ENST00000527992.5:n.301A>C
ENST00000529510.5:n.92A>C
ENST00000530407.5:n.197+96A>C
ENST00000532085.1:n.1568A>C
ENST00000532888.6:n.269A>C
ENST00000534384.1:n.294A>C
ENST00000538950.5:c.-172+96A>C	ENSP00000475991.2:n.-172+96A>C
ENST00000545985.5:c.74A>C	ENSP00000475241.2:p.Tyr25Ser
NM_001164277.1:c.74A>C , LRG_187t1:c.74A>C	NP_001157749.1:p.Tyr25Ser
NM_001164278.1:c.74A>C	NP_001157750.1:p.Tyr25Ser
NM_001164279.1:c.-172+96A>C	NP_001157751.1:n.-172+96A>C
NM_001164280.1:c.74A>C	NP_001157752.1:p.Tyr25Ser
NM_001467.5:c.74A>C	NP_001458.1:p.Tyr25Ser
NM_001164278.2:c.74A>C	NP_001157750.1:p.Tyr25Ser
NM_001164279.2:c.-172+96A>C	NP_001157751.1:n.-172+96A>C
NM_001164280.2:c.74A>C	NP_001157752.1:p.Tyr25Ser
NM_001467.6:c.74A>C	NP_001458.1:p.Tyr25Ser
NM_001164277.2:c.74A>C MANE Select	NP_001157749.1:p.Tyr25Ser