Canonical Allele Identifier: CA2003775423

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029419_119029420delinsAG , CM000673.2:g.119029419_119029420delinsAG	GRCh38
NC_000011.9:g.118900129_118900130delinsAG , CM000673.1:g.118900129_118900130delinsAG	GRCh37
NC_000011.8:g.118405339_118405340delinsAG	NCBI36
NG_013331.1:g.6487_6488delinsCT , LRG_187:g.6487_6488delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.179_180delinsCT
ENST00000697846.1:n.179_180delinsCT
ENST00000697847.1:n.179_180delinsCT
ENST00000697848.1:n.179_180delinsCT
ENST00000697849.1:n.423_424delinsCT
ENST00000697850.1:n.179_180delinsCT
ENST00000697851.1:n.423_424delinsCT
ENST00000638186.1:n.253_254delinsCT
ENST00000638360.1:n.187_188delinsCT
ENST00000638925.1:n.186_187delinsCT
ENST00000650539.1:n.355_356delinsCT
ENST00000330775.9:c.-51_-50delinsCT	ENSP00000476242.2:n.-51_-50delinsCT
ENST00000357590.9:c.-51_-50delinsCT	ENSP00000476176.2:n.-51_-50delinsCT
ENST00000525039.5:n.373_374delinsCT
ENST00000525102.5:n.707_708delinsCT
ENST00000525787.1:n.245_246delinsCT
ENST00000526626.6:n.145_146delinsCT
ENST00000527992.5:n.177_178delinsCT
ENST00000530407.5:n.169_170delinsCT
ENST00000532085.1:n.1444_1445delinsCT
ENST00000532888.6:n.145_146delinsCT
ENST00000534384.1:n.170_171delinsCT
ENST00000538950.5:c.-200_-199delinsCT	ENSP00000475991.2:n.-200_-199delinsCT
ENST00000545985.5:c.-51_-50delinsCT	ENSP00000475241.2:n.-51_-50delinsCT
NM_001164277.1:c.-51_-50delinsCT , LRG_187t1:c.-51_-50delinsCT	NP_001157749.1:n.-51_-50delinsCT
NM_001164278.1:c.-51_-50delinsCT	NP_001157750.1:n.-51_-50delinsCT
NM_001164279.1:c.-200_-199delinsCT	NP_001157751.1:n.-200_-199delinsCT
NM_001164280.1:c.-51_-50delinsCT	NP_001157752.1:n.-51_-50delinsCT
NM_001467.5:c.-51_-50delinsCT	NP_001458.1:n.-51_-50delinsCT
NM_001164278.2:c.-51_-50delinsCT	NP_001157750.1:n.-51_-50delinsCT
NM_001164279.2:c.-200_-199delinsCT	NP_001157751.1:n.-200_-199delinsCT
NM_001164280.2:c.-51_-50delinsCT	NP_001157752.1:n.-51_-50delinsCT
NM_001467.6:c.-51_-50delinsCT	NP_001458.1:n.-51_-50delinsCT
NM_001164277.2:c.-51_-50delinsCT MANE Select	NP_001157749.1:n.-51_-50delinsCT