Canonical Allele Identifier: CA1787849328

Gene: CA8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60222677C= , CM000670.2:g.60222677C=	GRCh38
NC_000008.10:g.61135236C= , CM000670.1:g.61135236C=	GRCh37
NC_000008.9:g.61297790C=	NCBI36
NG_023193.1:g.63719G=
NG_023193.2:g.63719G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004056.6:c.710G= MANE Select	NP_004047.3:p.Arg237=
ENST00000317995.5:c.710G= MANE Select	ENSP00000314407.4:p.Arg237=
NM_001321837.1:c.710G=	NP_001308766.1:p.Arg237=
NM_001321837.2:c.710G=	NP_001308766.1:p.Arg237=
NM_001321838.1:c.710G=	NP_001308767.1:p.Arg237=
NM_001321838.2:c.710G=	NP_001308767.1:p.Arg237=
NM_001321839.1:c.614G=	NP_001308768.1:p.Arg205=
NM_001321839.2:c.614G=	NP_001308768.1:p.Arg205=
NM_004056.4:c.710G=	NP_004047.3:p.Arg237=
NM_004056.5:c.710G=	NP_004047.3:p.Arg237=
NR_135821.1:n.986G=
NR_135821.2:n.963G=
ENST00000317995.4:c.710G=	ENSP00000314407.4:p.Arg237=
ENST00000524872.5:n.948G=
ENST00000528666.1:n.482G=
XM_011517585.1:c.710G=	XP_011515887.1:p.Arg237=
XM_011517586.1:c.614G=	XP_011515888.1:p.Arg205=
XM_017013818.1:c.458G=	XP_016869307.1:p.Arg153=