Canonical Allele Identifier: CA2003748255

Gene: SLC37A4 TRAPPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024943G= , CM000673.2:g.119024943G=	GRCh38
NC_000011.9:g.118895653G= , CM000673.1:g.118895653G=	GRCh37
NC_000011.8:g.118400863G=	NCBI36
NG_013331.1:g.10963C= , LRG_187:g.10963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1467C= (SLC37A4)
ENST00000697845.1:n.2456C= (SLC37A4)
ENST00000697846.1:n.1829C= (SLC37A4)
ENST00000697847.1:n.1540C= (SLC37A4)
ENST00000697849.1:n.3933C= (SLC37A4)
ENST00000697850.1:n.2124C= (SLC37A4)
ENST00000697851.1:n.3095C= (SLC37A4)
ENST00000638186.1:n.1561C= (SLC37A4)
ENST00000638360.1:n.1393C= (SLC37A4)
ENST00000638925.1:n.1526C= (SLC37A4)
ENST00000650539.1:n.1729C= (SLC37A4)
ENST00000330775.9:c.1257C= (SLC37A4)	ENSP00000476242.2:p.Thr419=
ENST00000357590.9:c.1323C= (SLC37A4)	ENSP00000476176.2:p.Thr441=
ENST00000524428.5:n.1493C= (SLC37A4)
ENST00000525039.5:n.1747C= (SLC37A4)
ENST00000525102.5:n.2015C= (SLC37A4)
ENST00000525372.5:n.1355C= (SLC37A4)
ENST00000526275.5:n.2039C= (SLC37A4)
ENST00000527992.5:n.1485C= (SLC37A4)
ENST00000530407.5:n.1407C= (SLC37A4)
ENST00000532085.1:n.5275C= (SLC37A4)
ENST00000533058.5:c.668G= (TRAPPC4)	ENSP00000432920.1:p.Trp223=
ENST00000538950.5:c.1038C= (SLC37A4)	ENSP00000475991.2:p.Thr346=
ENST00000545985.5:c.1257C= (SLC37A4)	ENSP00000475241.2:p.Thr419=
NM_001164277.1:c.1257C= , LRG_187t1:c.1257C= (SLC37A4)	NP_001157749.1:p.Thr419=
NM_001164278.1:c.1323C= (SLC37A4)	NP_001157750.1:p.Thr441=
NM_001164279.1:c.1038C= (SLC37A4)	NP_001157751.1:p.Thr346=
NM_001164280.1:c.1257C= (SLC37A4)	NP_001157752.1:p.Thr419=
NM_001467.5:c.1257C= (SLC37A4)	NP_001458.1:p.Thr419=
NM_001164278.2:c.1323C= (SLC37A4)	NP_001157750.1:p.Thr441=
NM_001164279.2:c.1038C= (SLC37A4)	NP_001157751.1:p.Thr346=
NM_001164280.2:c.1257C= (SLC37A4)	NP_001157752.1:p.Thr419=
NM_001467.6:c.1257C= (SLC37A4)	NP_001458.1:p.Thr419=
NM_001164277.2:c.1257C= (SLC37A4) MANE Select	NP_001157749.1:p.Thr419=