Canonical Allele Identifier: CA2003749143

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026642G= , CM000673.2:g.119026642G=	GRCh38
NC_000011.9:g.118897352G= , CM000673.1:g.118897352G=	GRCh37
NC_000011.8:g.118402562G=	NCBI36
NG_013331.1:g.9264C= , LRG_187:g.9264C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+295C=
ENST00000697845.1:n.1233C=
ENST00000697846.1:n.1014+295C=
ENST00000697847.1:n.1061C=
ENST00000697848.1:n.1061C=
ENST00000697849.1:n.2348C=
ENST00000697850.1:n.1061C=
ENST00000697851.1:n.2669C=
ENST00000638186.1:n.1135C=
ENST00000638360.1:n.967C=
ENST00000638925.1:n.1068C=
ENST00000650539.1:n.1237C=
ENST00000330775.9:c.831C=	ENSP00000476242.2:p.Ser277=
ENST00000357590.9:c.831C=	ENSP00000476176.2:p.Ser277=
ENST00000524428.5:n.1106+295C=
ENST00000525039.5:n.1255C=
ENST00000525102.5:n.1589C=
ENST00000525372.5:n.832C=
ENST00000526275.5:n.1613C=
ENST00000527992.5:n.1059C=
ENST00000529510.5:n.558+295C=
ENST00000530407.5:n.981C=
ENST00000532085.1:n.3690C=
ENST00000538950.5:c.612C=	ENSP00000475991.2:p.Ser204=
ENST00000545985.5:c.831C=	ENSP00000475241.2:p.Ser277=
NM_001164277.1:c.831C= , LRG_187t1:c.831C=	NP_001157749.1:p.Ser277=
NM_001164278.1:c.831C=	NP_001157750.1:p.Ser277=
NM_001164279.1:c.612C=	NP_001157751.1:p.Ser204=
NM_001164280.1:c.831C=	NP_001157752.1:p.Ser277=
NM_001467.5:c.831C=	NP_001458.1:p.Ser277=
NM_001164278.2:c.831C=	NP_001157750.1:p.Ser277=
NM_001164279.2:c.612C=	NP_001157751.1:p.Ser204=
NM_001164280.2:c.831C=	NP_001157752.1:p.Ser277=
NM_001467.6:c.831C=	NP_001458.1:p.Ser277=
NM_001164277.2:c.831C= MANE Select	NP_001157749.1:p.Ser277=