Canonical Allele Identifier: CA2322525555

Gene: SLC44A2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631078T= , CM000681.2:g.10631078T=	GRCh38
NC_000019.9:g.10741754T= , CM000681.1:g.10741754T=	GRCh37
NC_000019.8:g.10602754T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.267T= MANE Select	ENSP00000336888.4:p.Tyr89=
ENST00000335757.9:c.267T=	ENSP00000336888.4:p.Tyr89=
ENST00000407327.8:c.261T=	ENSP00000385135.3:p.Tyr87=
ENST00000586078.5:c.267T=	ENSP00000466664.1:p.Tyr89=
ENST00000588409.1:c.245+3074T=	ENSP00000468070.1:n.245+3074T=
ENST00000588465.5:n.176T=
ENST00000588688.5:c.108T=	ENSP00000467552.1:p.Tyr36=
ENST00000590382.5:c.102T=	ENSP00000468691.1:p.Tyr34=
ENST00000590857.5:c.-283T=	ENSP00000465547.1:n.-283T=
ENST00000592293.5:c.*64T=	ENSP00000466612.1:n.*64T=
NM_001145056.1:c.261T=	NP_001138528.1:p.Tyr87=
NM_020428.3:c.267T=	NP_065161.3:p.Tyr89=
XM_005259997.1:c.267T=	XP_005260054.1:p.Tyr89=
XM_005259999.1:c.261T=	XP_005260056.1:p.Tyr87=
NM_001363611.1:c.267T=	NP_001350540.1:p.Tyr89=
XM_005259999.2:c.261T=	XP_005260056.1:p.Tyr87=
NM_020428.4:c.267T= MANE Select	NP_065161.3:p.Tyr89=
NM_001145056.2:c.261T=	NP_001138528.1:p.Tyr87=
NM_001363611.2:c.267T=	NP_001350540.1:p.Tyr89=