Canonical Allele Identifier: CA2975984968

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029378A>G , CM000673.2:g.119029378A>G	GRCh38
NC_000011.9:g.118900088A>G , CM000673.1:g.118900088A>G	GRCh37
NC_000011.8:g.118405298A>G	NCBI36
NG_013331.1:g.6529T>C , LRG_187:g.6529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.221T>C
ENST00000697846.1:n.221T>C
ENST00000697847.1:n.221T>C
ENST00000697848.1:n.221T>C
ENST00000697849.1:n.465T>C
ENST00000697850.1:n.221T>C
ENST00000697851.1:n.465T>C
ENST00000638186.1:n.295T>C
ENST00000638360.1:n.229T>C
ENST00000638925.1:n.228T>C
ENST00000650539.1:n.397T>C
ENST00000330775.9:c.-9T>C	ENSP00000476242.2:n.-9T>C
ENST00000357590.9:c.-9T>C	ENSP00000476176.2:n.-9T>C
ENST00000525039.5:n.415T>C
ENST00000525102.5:n.749T>C
ENST00000525787.1:n.287T>C
ENST00000526626.6:n.187T>C
ENST00000527992.5:n.219T>C
ENST00000529510.5:n.10T>C
ENST00000530407.5:n.197+14T>C
ENST00000532085.1:n.1486T>C
ENST00000532888.6:n.187T>C
ENST00000534384.1:n.212T>C
ENST00000538950.5:c.-172+14T>C	ENSP00000475991.2:n.-172+14T>C
ENST00000545985.5:c.-9T>C	ENSP00000475241.2:n.-9T>C
NM_001164277.1:c.-9T>C , LRG_187t1:c.-9T>C	NP_001157749.1:n.-9T>C
NM_001164278.1:c.-9T>C	NP_001157750.1:n.-9T>C
NM_001164279.1:c.-172+14T>C	NP_001157751.1:n.-172+14T>C
NM_001164280.1:c.-9T>C	NP_001157752.1:n.-9T>C
NM_001467.5:c.-9T>C	NP_001458.1:n.-9T>C
NM_001164278.2:c.-9T>C	NP_001157750.1:n.-9T>C
NM_001164279.2:c.-172+14T>C	NP_001157751.1:n.-172+14T>C
NM_001164280.2:c.-9T>C	NP_001157752.1:n.-9T>C
NM_001467.6:c.-9T>C	NP_001458.1:n.-9T>C
NM_001164277.2:c.-9T>C MANE Select	NP_001157749.1:n.-9T>C