Canonical Allele Identifier: CA404018157

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10741798T>G (hg19) ; chr19:g.10631122T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631122T>G , CM000681.2:g.10631122T>G	GRCh38
NC_000019.9:g.10741798T>G , CM000681.1:g.10741798T>G	GRCh37
NC_000019.8:g.10602798T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.311T>G MANE Select	ENSP00000336888.4:p.Phe104Cys
ENST00000335757.9:c.311T>G	ENSP00000336888.4:p.Phe104Cys
ENST00000407327.8:c.305T>G	ENSP00000385135.3:p.Phe102Cys
ENST00000586078.5:c.311T>G	ENSP00000466664.1:p.Phe104Cys
ENST00000588409.1:c.245+3118T>G	ENSP00000468070.1:n.245+3118T>G
ENST00000588465.5:n.220T>G
ENST00000588688.5:c.152T>G	ENSP00000467552.1:p.Phe51Cys
ENST00000590382.5:c.146T>G	ENSP00000468691.1:p.Phe49Cys
ENST00000590857.5:c.-239T>G	ENSP00000465547.1:n.-239T>G
ENST00000592293.5:c.*108T>G	ENSP00000466612.1:n.*108T>G
NM_001145056.1:c.305T>G	NP_001138528.1:p.Phe102Cys
NM_020428.3:c.311T>G	NP_065161.3:p.Phe104Cys
XM_005259997.1:c.311T>G	XP_005260054.1:p.Phe104Cys
XM_005259999.1:c.305T>G	XP_005260056.1:p.Phe102Cys
NM_001363611.1:c.311T>G	NP_001350540.1:p.Phe104Cys
XM_005259999.2:c.305T>G	XP_005260056.1:p.Phe102Cys
NM_020428.4:c.311T>G MANE Select	NP_065161.3:p.Phe104Cys
NM_001145056.2:c.305T>G	NP_001138528.1:p.Phe102Cys
NM_001363611.2:c.311T>G	NP_001350540.1:p.Phe104Cys