Canonical Allele Identifier: CA404019326

Gene: SLC44A2

Linked Data

• MyVariant Identifiers: chr19:g.10742172G>T (hg19) ; chr19:g.10631496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10631496G>T , CM000681.2:g.10631496G>T	GRCh38
NC_000019.9:g.10742172G>T , CM000681.1:g.10742172G>T	GRCh37
NC_000019.8:g.10603172G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335757.10:c.463G>T MANE Select	ENSP00000336888.4:p.Asp155Tyr
ENST00000335757.9:c.463G>T	ENSP00000336888.4:p.Asp155Tyr
ENST00000407327.8:c.457G>T	ENSP00000385135.3:p.Asp153Tyr
ENST00000586078.5:c.463G>T	ENSP00000466664.1:p.Asp155Tyr
ENST00000588409.1:c.246-3260G>T	ENSP00000468070.1:n.246-3260G>T
ENST00000588465.5:n.372G>T
ENST00000588688.5:c.304G>T	ENSP00000467552.1:p.Asp102Tyr
ENST00000590382.5:c.298G>T	ENSP00000468691.1:p.Asp100Tyr
ENST00000590857.5:c.-87G>T	ENSP00000465547.1:n.-87G>T
ENST00000592293.5:c.*260G>T	ENSP00000466612.1:n.*260G>T
NM_001145056.1:c.457G>T	NP_001138528.1:p.Asp153Tyr
NM_020428.3:c.463G>T	NP_065161.3:p.Asp155Tyr
XM_005259997.1:c.463G>T	XP_005260054.1:p.Asp155Tyr
XM_005259999.1:c.457G>T	XP_005260056.1:p.Asp153Tyr
NM_001363611.1:c.463G>T	NP_001350540.1:p.Asp155Tyr
XM_005259999.2:c.457G>T	XP_005260056.1:p.Asp153Tyr
NM_020428.4:c.463G>T MANE Select	NP_065161.3:p.Asp155Tyr
NM_001145056.2:c.457G>T	NP_001138528.1:p.Asp153Tyr
NM_001363611.2:c.463G>T	NP_001350540.1:p.Asp155Tyr