Canonical Allele Identifier: CA382901514

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897764A>G (hg19) ; chr11:g.119027054A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027054A>G , CM000673.2:g.119027054A>G	GRCh38
NC_000011.9:g.118897764A>G , CM000673.1:g.118897764A>G	GRCh37
NC_000011.8:g.118402974A>G	NCBI36
NG_013331.1:g.8852T>C , LRG_187:g.8852T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.897T>C
ENST00000697845.1:n.821T>C
ENST00000697846.1:n.897T>C
ENST00000697847.1:n.897T>C
ENST00000697848.1:n.897T>C
ENST00000697849.1:n.1936T>C
ENST00000697850.1:n.897T>C
ENST00000697851.1:n.2257T>C
ENST00000638186.1:n.971T>C
ENST00000638360.1:n.803T>C
ENST00000638925.1:n.904T>C
ENST00000650539.1:n.1073T>C
ENST00000330775.9:c.667T>C	ENSP00000476242.2:p.Ser223Pro
ENST00000357590.9:c.667T>C	ENSP00000476176.2:p.Ser223Pro
ENST00000524428.5:n.989T>C
ENST00000525039.5:n.1091T>C
ENST00000525102.5:n.1425T>C
ENST00000525372.5:n.668T>C
ENST00000526275.5:n.1449T>C
ENST00000526626.6:n.630T>C
ENST00000527992.5:n.895T>C
ENST00000529510.5:n.441T>C
ENST00000530407.5:n.817T>C
ENST00000532085.1:n.3278T>C
ENST00000532888.6:n.963T>C
ENST00000538950.5:c.448T>C	ENSP00000475991.2:p.Ser150Pro
ENST00000545985.5:c.667T>C	ENSP00000475241.2:p.Ser223Pro
NM_001164277.1:c.667T>C , LRG_187t1:c.667T>C	NP_001157749.1:p.Ser223Pro
NM_001164278.1:c.667T>C	NP_001157750.1:p.Ser223Pro
NM_001164279.1:c.448T>C	NP_001157751.1:p.Ser150Pro
NM_001164280.1:c.667T>C	NP_001157752.1:p.Ser223Pro
NM_001467.5:c.667T>C	NP_001458.1:p.Ser223Pro
NM_001164278.2:c.667T>C	NP_001157750.1:p.Ser223Pro
NM_001164279.2:c.448T>C	NP_001157751.1:p.Ser150Pro
NM_001164280.2:c.667T>C	NP_001157752.1:p.Ser223Pro
NM_001467.6:c.667T>C	NP_001458.1:p.Ser223Pro
NM_001164277.2:c.667T>C MANE Select	NP_001157749.1:p.Ser223Pro