Canonical Allele Identifier: CA3195756747

Gene: CRACR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3630668G>A , CM000674.2:g.3630668G>A	GRCh38
NC_000012.11:g.3739834G>A , CM000674.1:g.3739834G>A	GRCh37
NC_000012.10:g.3610095G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001144958.2:c.1735+2936C>T MANE Select	NP_001138430.1:n.1735+2936C>T
ENST00000440314.7:c.1735+2936C>T MANE Select	ENSP00000409382.2:n.1735+2936C>T
NM_001144958.1:c.1735+2936C>T	NP_001138430.1:n.1735+2936C>T
ENST00000333750.9:c.1328+2936C>T
ENST00000440314.6:c.1735+2936C>T	ENSP00000409382.2:n.1735+2936C>T
XM_006719021.2:c.1738+2936C>T	XP_006719084.1:n.1738+2936C>T
XM_006719021.3:c.1738+2936C>T	XP_006719084.1:n.1738+2936C>T
XM_011521034.1:c.1738+2936C>T	XP_011519336.1:n.1738+2936C>T
XM_011521034.3:c.1738+2936C>T	XP_011519336.1:n.1738+2936C>T
XM_011521035.1:c.1738+2936C>T	XP_011519337.1:n.1738+2936C>T
XM_011521036.1:c.1738+2936C>T	XP_011519338.1:n.1738+2936C>T
XM_011521036.3:c.1738+2936C>T	XP_011519338.1:n.1738+2936C>T
XM_011521037.1:c.1021+2936C>T	XP_011519339.1:n.1021+2936C>T
XM_011521037.2:c.1021+2936C>T	XP_011519339.1:n.1021+2936C>T
XM_011521038.1:c.1021+2936C>T	XP_011519340.1:n.1021+2936C>T
XM_011521038.2:c.1021+2936C>T	XP_011519340.1:n.1021+2936C>T