Canonical Allele Identifier: CA602797583

Gene: CRACR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3680942_3680947dup , CM000674.2:g.3680942_3680947dup	GRCh38
NC_000012.11:g.3790108_3790113dup , CM000674.1:g.3790108_3790113dup	GRCh37
NC_000012.10:g.3660369_3660374dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001144958.2:c.229-589_229-584dup MANE Select	NP_001138430.1:n.229-589_229-584dup
ENST00000440314.7:c.229-589_229-584dup MANE Select	ENSP00000409382.2:n.229-589_229-584dup
NM_001144958.1:c.229-589_229-584dup	NP_001138430.1:n.229-589_229-584dup
NM_032680.3:c.229-589_229-584dup	NP_116069.1:n.229-589_229-584dup
NM_032680.4:c.229-589_229-584dup	NP_116069.1:n.229-589_229-584dup
ENST00000252322.1:c.229-589_229-584dup	ENSP00000252322.1:n.229-589_229-584dup
ENST00000440314.6:c.229-589_229-584dup	ENSP00000409382.2:n.229-589_229-584dup
XM_006719021.2:c.229-589_229-584dup	XP_006719084.1:n.229-589_229-584dup
XM_006719021.3:c.229-589_229-584dup	XP_006719084.1:n.229-589_229-584dup
XM_011521034.1:c.229-589_229-584dup	XP_011519336.1:n.229-589_229-584dup
XM_011521034.3:c.229-589_229-584dup	XP_011519336.1:n.229-589_229-584dup
XM_011521035.1:c.229-589_229-584dup	XP_011519337.1:n.229-589_229-584dup
XM_011521036.1:c.229-589_229-584dup	XP_011519338.1:n.229-589_229-584dup
XM_011521036.3:c.229-589_229-584dup	XP_011519338.1:n.229-589_229-584dup