Canonical Allele Identifier: CA382904476

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898914A>G (hg19) ; chr11:g.119028204A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028204A>G , CM000673.2:g.119028204A>G	GRCh38
NC_000011.9:g.118898914A>G , CM000673.1:g.118898914A>G	GRCh37
NC_000011.8:g.118404124A>G	NCBI36
NG_013331.1:g.7703T>C , LRG_187:g.7703T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.600T>C
ENST00000697845.1:n.524T>C
ENST00000697846.1:n.600T>C
ENST00000697847.1:n.600T>C
ENST00000697848.1:n.600T>C
ENST00000697849.1:n.1639T>C
ENST00000697850.1:n.600T>C
ENST00000697851.1:n.1639T>C
ENST00000638186.1:n.674T>C
ENST00000638360.1:n.608T>C
ENST00000638925.1:n.607T>C
ENST00000650539.1:n.776T>C
ENST00000330775.9:c.371T>C	ENSP00000476242.2:p.Val124Ala
ENST00000357590.9:c.371T>C	ENSP00000476176.2:p.Val124Ala
ENST00000524428.5:n.371T>C
ENST00000525039.5:n.794T>C
ENST00000525102.5:n.1128T>C
ENST00000525372.5:n.371T>C
ENST00000525787.1:n.666T>C
ENST00000526275.5:n.831T>C
ENST00000526626.6:n.344-332T>C
ENST00000527992.5:n.598T>C
ENST00000529510.5:n.389T>C
ENST00000530407.5:n.520T>C
ENST00000532085.1:n.2660T>C
ENST00000532888.6:n.666T>C
ENST00000538950.5:c.152T>C	ENSP00000475991.2:p.Val51Ala
ENST00000545985.5:c.371T>C	ENSP00000475241.2:p.Val124Ala
NM_001164277.1:c.371T>C , LRG_187t1:c.371T>C	NP_001157749.1:p.Val124Ala
NM_001164278.1:c.371T>C	NP_001157750.1:p.Val124Ala
NM_001164279.1:c.152T>C	NP_001157751.1:p.Val51Ala
NM_001164280.1:c.371T>C	NP_001157752.1:p.Val124Ala
NM_001467.5:c.371T>C	NP_001458.1:p.Val124Ala
NM_001164278.2:c.371T>C	NP_001157750.1:p.Val124Ala
NM_001164279.2:c.152T>C	NP_001157751.1:p.Val51Ala
NM_001164280.2:c.371T>C	NP_001157752.1:p.Val124Ala
NM_001467.6:c.371T>C	NP_001458.1:p.Val124Ala
NM_001164277.2:c.371T>C MANE Select	NP_001157749.1:p.Val124Ala