Canonical Allele Identifier: CA1619332368

Gene: SLC44A4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31866420C= , CM000668.2:g.31866420C=	GRCh38
NC_000006.11:g.31834197C= , CM000668.1:g.31834197C=	GRCh37
NC_000006.10:g.31942176C=	NCBI36
NG_008201.1:g.1513G=
NG_023058.1:g.17627G=

Transcript Alleles

HGVS	Amino-acid Change
NM_025257.3:c.1234-294G= MANE Select	NP_079533.2:n.1234-294G=
ENST00000229729.11:c.1234-294G= MANE Select	ENSP00000229729.6:n.1234-294G=
NM_001178044.1:c.1108-294G=	NP_001171515.1:n.1108-294G=
NM_001178044.2:c.1108-294G=	NP_001171515.1:n.1108-294G=
NM_001178045.1:c.1006-294G=	NP_001171516.1:n.1006-294G=
NM_001178045.2:c.1006-294G=	NP_001171516.1:n.1006-294G=
NM_025257.2:c.1234-294G=	NP_079533.2:n.1234-294G=
ENST00000229729.10:c.1234-294G=	ENSP00000229729.6:n.1234-294G=
ENST00000375562.8:c.1108-294G=	ENSP00000364712.4:n.1108-294G=
ENST00000414427.1:c.885-294G=
ENST00000479777.1:n.588-294G=
ENST00000544672.5:c.1006-294G=	ENSP00000444109.1:n.1006-294G=