Canonical Allele Identifier: CA13758050

Gene: CRACR2A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3705072G>A , CM000674.2:g.3705072G>A	GRCh38
NC_000012.11:g.3814238G>A , CM000674.1:g.3814238G>A	GRCh37
NC_000012.10:g.3684499G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440314.7:c.-36-8037C>T MANE Select	ENSP00000409382.2:n.-36-8037C>T
ENST00000252322.1:c.-36-8037C>T	ENSP00000252322.1:n.-36-8037C>T
ENST00000440314.6:c.-36-8037C>T	ENSP00000409382.2:n.-36-8037C>T
NM_001144958.1:c.-36-8037C>T	NP_001138430.1:n.-36-8037C>T
NM_032680.3:c.-36-8037C>T	NP_116069.1:n.-36-8037C>T
XM_006719021.2:c.-36-8037C>T	XP_006719084.1:n.-36-8037C>T
XM_011521034.1:c.-36-8037C>T	XP_011519336.1:n.-36-8037C>T
XM_011521035.1:c.-36-8037C>T	XP_011519337.1:n.-36-8037C>T
XM_006719021.3:c.-36-8037C>T	XP_006719084.1:n.-36-8037C>T
XM_011521034.3:c.-36-8037C>T	XP_011519336.1:n.-36-8037C>T
NM_001144958.2:c.-36-8037C>T MANE Select	NP_001138430.1:n.-36-8037C>T
NM_032680.4:c.-36-8037C>T	NP_116069.1:n.-36-8037C>T