Canonical Allele Identifier: CA7953902

Gene: UQCRC2 PDZD9

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21972152T>C , CM000678.2:g.21972152T>C	GRCh38
NC_000016.9:g.21983473T>C , CM000678.1:g.21983473T>C	GRCh37
NC_000016.8:g.21890974T>C	NCBI36
NG_042228.1:g.24089T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003366.4:c.966+30T>C (UQCRC2) MANE Select	NP_003357.2:n.966+30T>C
ENST00000268379.9:c.966+30T>C (UQCRC2) MANE Select	ENSP00000268379.4:n.966+30T>C
NM_003366.2:c.966+30T>C (UQCRC2)	NP_003357.2:n.966+30T>C
NM_003366.3:c.966+30T>C (UQCRC2)	NP_003357.2:n.966+30T>C
ENST00000268379.8:c.966+30T>C (UQCRC2)	ENSP00000268379.4:n.966+30T>C
ENST00000561553.5:c.966+30T>C (UQCRC2)	ENSP00000456232.1:n.966+30T>C
ENST00000563711.5:n.1146+30T>C (UQCRC2)
ENST00000563898.5:c.966+30T>C (UQCRC2)	ENSP00000456738.1:n.966+30T>C
ENST00000567810.1:n.520+30T>C (UQCRC2)
XM_011545785.1:c.786+12124A>G (PDZD9)	XP_011544087.1:n.786+12124A>G
XM_011545785.3:c.786+12124A>G (PDZD9)	XP_011544087.1:n.786+12124A>G
XM_017023109.1:c.606+12124A>G (PDZD9)	XP_016878598.1:n.606+12124A>G
XM_017023110.1:c.600+12124A>G (PDZD9)	XP_016878599.1:n.600+12124A>G