Canonical Allele Identifier: CA2264592558

Gene: CA10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.51653013A= , CM000679.2:g.51653013A=	GRCh38
NC_000017.10:g.49730374A= , CM000679.1:g.49730374A=	GRCh37
NC_000017.9:g.47085373A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000451037.7:c.561+628T= MANE Select	ENSP00000405388.2:n.561+628T=
ENST00000285273.8:c.561+628T=	ENSP00000285273.4:n.561+628T=
ENST00000442502.6:c.561+628T=	ENSP00000390666.2:n.561+628T=
ENST00000451037.6:c.561+628T=	ENSP00000405388.2:n.561+628T=
ENST00000570565.5:c.336+628T=	ENSP00000459619.1:n.336+628T=
ENST00000571371.5:c.*603+628T=	ENSP00000461908.1:n.*603+628T=
ENST00000571918.1:n.400+628T=
ENST00000575181.1:c.561+628T=	ENSP00000460238.1:n.561+628T=
NM_001082533.1:c.561+628T=	NP_001076002.1:n.561+628T=
NM_001082534.1:c.561+628T=	NP_001076003.1:n.561+628T=
NM_020178.4:c.561+628T=	NP_064563.1:n.561+628T=
XR_934507.1:n.401+628T=
XM_017024878.2:c.270+628T=	XP_016880367.1:n.270+628T=
NM_020178.5:c.561+628T= MANE Select	NP_064563.1:n.561+628T=
NM_001082534.2:c.561+628T=	NP_001076003.1:n.561+628T=