Canonical Allele Identifier: CA2609360359

Gene: DNAJC12

Linked Data

• gnomAD v4: 10-67811685-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811685G>A , CM000672.2:g.67811685G>A	GRCh38
NC_000010.10:g.69571443G>A , CM000672.1:g.69571443G>A	GRCh37
NC_000010.9:g.69241449G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.158-22C>T MANE Select	ENSP00000225171.2:n.158-22C>T
ENST00000225171.6:c.158-22C>T	ENSP00000225171.2:n.158-22C>T
ENST00000339758.7:c.158-22C>T	ENSP00000343575.6:n.158-22C>T
ENST00000480180.1:c.*177-22C>T	ENSP00000474804.1:n.*177-22C>T
ENST00000480963.5:c.*78-22C>T	ENSP00000473979.1:n.*78-22C>T
ENST00000483798.6:c.248-22C>T	ENSP00000474215.1:n.248-22C>T
NM_021800.2:c.158-22C>T	NP_068572.1:n.158-22C>T
NM_201262.1:c.158-22C>T	NP_957714.1:n.158-22C>T
XM_011539967.1:c.188-22C>T	XP_011538269.1:n.188-22C>T
XM_017016431.1:c.-89-22C>T	XP_016871920.1:n.-89-22C>T
XM_017016432.2:c.-89-22C>T	XP_016871921.1:n.-89-22C>T
NM_021800.3:c.158-22C>T MANE Select	NP_068572.1:n.158-22C>T
NM_201262.2:c.158-22C>T	NP_957714.1:n.158-22C>T