Canonical Allele Identifier: CA3725827

Gene: SLC44A4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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