Canonical Allele Identifier: CA1619336454

Gene: SLC44A4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31871532C= , CM000668.2:g.31871532C=	GRCh38
NC_000006.11:g.31839309C= , CM000668.1:g.31839309C=	GRCh37
NC_000006.10:g.31947288C=	NCBI36
NG_023058.1:g.12515G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229729.11:c.559G= MANE Select	ENSP00000229729.6:p.Val187=
ENST00000229729.10:c.559G=	ENSP00000229729.6:p.Val187=
ENST00000375562.8:c.433G=	ENSP00000364712.4:p.Val145=
ENST00000414427.1:c.546G=
ENST00000544672.5:c.331G=	ENSP00000444109.1:p.Val111=
NM_001178044.1:c.433G=	NP_001171515.1:p.Val145=
NM_001178045.1:c.331G=	NP_001171516.1:p.Val111=
NM_025257.2:c.559G=	NP_079533.2:p.Val187=
NM_025257.3:c.559G= MANE Select	NP_079533.2:p.Val187=
NM_001178044.2:c.433G=	NP_001171515.1:p.Val145=
NM_001178045.2:c.331G=	NP_001171516.1:p.Val111=