Canonical Allele Identifier: CA602577853
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs1457293197

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029406A>G , CM000673.2:g.119029406A>G GRCh38
NC_000011.9:g.118900116A>G , CM000673.1:g.118900116A>G GRCh37
NC_000011.8:g.118405326A>G NCBI36
NG_013331.1:g.6501T>C , LRG_187:g.6501T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.193T>C
ENST00000697846.1:n.193T>C
ENST00000697847.1:n.193T>C
ENST00000697848.1:n.193T>C
ENST00000697849.1:n.437T>C
ENST00000697850.1:n.193T>C
ENST00000697851.1:n.437T>C
ENST00000638186.1:n.267T>C
ENST00000638360.1:n.201T>C
ENST00000638925.1:n.200T>C
ENST00000650539.1:n.369T>C
ENST00000330775.9:c.-37T>C ENSP00000476242.2:n.-37T>C
ENST00000357590.9:c.-37T>C ENSP00000476176.2:n.-37T>C
ENST00000525039.5:n.387T>C
ENST00000525102.5:n.721T>C
ENST00000525787.1:n.259T>C
ENST00000526626.6:n.159T>C
ENST00000527992.5:n.191T>C
ENST00000530407.5:n.183T>C
ENST00000532085.1:n.1458T>C
ENST00000532888.6:n.159T>C
ENST00000534384.1:n.184T>C
ENST00000538950.5:c.-186T>C ENSP00000475991.2:n.-186T>C
ENST00000545985.5:c.-37T>C ENSP00000475241.2:n.-37T>C
NM_001164277.1:c.-37T>C , LRG_187t1:c.-37T>C NP_001157749.1:n.-37T>C
NM_001164278.1:c.-37T>C NP_001157750.1:n.-37T>C
NM_001164279.1:c.-186T>C NP_001157751.1:n.-186T>C
NM_001164280.1:c.-37T>C NP_001157752.1:n.-37T>C
NM_001467.5:c.-37T>C NP_001458.1:n.-37T>C
NM_001164278.2:c.-37T>C NP_001157750.1:n.-37T>C
NM_001164279.2:c.-186T>C NP_001157751.1:n.-186T>C
NM_001164280.2:c.-37T>C NP_001157752.1:n.-37T>C
NM_001467.6:c.-37T>C NP_001458.1:n.-37T>C
NM_001164277.2:c.-37T>C MANE Select NP_001157749.1:n.-37T>C