Canonical Allele Identifier: CA2788369903

Gene: DNAJC12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811722A>C , CM000672.2:g.67811722A>C	GRCh38
NC_000010.10:g.69571480A>C , CM000672.1:g.69571480A>C	GRCh37
NC_000010.9:g.69241486A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.158-59T>G MANE Select	ENSP00000225171.2:n.158-59T>G
ENST00000225171.6:c.158-59T>G	ENSP00000225171.2:n.158-59T>G
ENST00000339758.7:c.158-59T>G	ENSP00000343575.6:n.158-59T>G
ENST00000480180.1:c.*177-59T>G	ENSP00000474804.1:n.*177-59T>G
ENST00000480963.5:c.*78-59T>G	ENSP00000473979.1:n.*78-59T>G
ENST00000483798.6:c.248-59T>G	ENSP00000474215.1:n.248-59T>G
NM_021800.2:c.158-59T>G	NP_068572.1:n.158-59T>G
NM_201262.1:c.158-59T>G	NP_957714.1:n.158-59T>G
XM_011539967.1:c.188-59T>G	XP_011538269.1:n.188-59T>G
XM_017016431.1:c.-89-59T>G	XP_016871920.1:n.-89-59T>G
XM_017016432.2:c.-89-59T>G	XP_016871921.1:n.-89-59T>G
NM_021800.3:c.158-59T>G MANE Select	NP_068572.1:n.158-59T>G
NM_201262.2:c.158-59T>G	NP_957714.1:n.158-59T>G