Canonical Allele Identifier: CA1619346616

Gene: SLC44A4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31876147C= , CM000668.2:g.31876147C=	GRCh38
NC_000006.11:g.31843924C= , CM000668.1:g.31843924C=	GRCh37
NC_000006.10:g.31951903C=	NCBI36
NG_023058.1:g.7900G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229729.11:c.90-18G= MANE Select	ENSP00000229729.6:n.90-18G=
ENST00000229729.10:c.90-18G=	ENSP00000229729.6:n.90-18G=
ENST00000375562.8:c.90-18G=	ENSP00000364712.4:n.90-18G=
ENST00000414427.1:c.77-18G=
ENST00000462671.1:n.107-18G=
ENST00000465707.5:n.107-18G=
ENST00000544672.5:c.-139-18G=	ENSP00000444109.1:n.-139-18G=
NM_001178044.1:c.90-18G=	NP_001171515.1:n.90-18G=
NM_001178045.1:c.-139-18G=	NP_001171516.1:n.-139-18G=
NM_025257.2:c.90-18G=	NP_079533.2:n.90-18G=
NM_025257.3:c.90-18G= MANE Select	NP_079533.2:n.90-18G=
NM_001178044.2:c.90-18G=	NP_001171515.1:n.90-18G=
NM_001178045.2:c.-139-18G=	NP_001171516.1:n.-139-18G=