Canonical Allele Identifier: CA15437015

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107211956T>G , CM000668.2:g.107211956T>G	GRCh38
NC_000006.11:g.107533160T>G , CM000668.1:g.107533160T>G	GRCh37
NC_000006.10:g.107639853T>G	NCBI36
NG_013033.1:g.252620A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020381.4:c.876+153A>C MANE Select	NP_065114.3:n.876+153A>C
ENST00000369037.9:c.876+153A>C MANE Select	ENSP00000358033.4:n.876+153A>C
NM_020381.3:c.876+153A>C	NP_065114.3:n.876+153A>C
ENST00000369037.8:c.876+153A>C	ENSP00000358033.4:n.876+153A>C
ENST00000449027.1:c.51+153A>C	ENSP00000392613.1:n.51+153A>C
XM_011535956.1:c.876+153A>C	XP_011534258.1:n.876+153A>C
XM_011535956.3:c.876+153A>C	XP_011534258.1:n.876+153A>C
XM_011535957.1:c.876+153A>C	XP_011534259.1:n.876+153A>C
XM_011535957.3:c.876+153A>C	XP_011534259.1:n.876+153A>C
XM_011535958.1:c.741+153A>C	XP_011534260.1:n.741+153A>C
XM_011535958.3:c.741+153A>C	XP_011534260.1:n.741+153A>C
XM_011535959.1:c.876+153A>C	XP_011534261.1:n.876+153A>C
XM_011535959.3:c.876+153A>C	XP_011534261.1:n.876+153A>C
XM_011535960.1:c.468+153A>C	XP_011534262.1:n.468+153A>C
XM_011535960.3:c.468+153A>C	XP_011534262.1:n.468+153A>C
XM_011535961.1:c.703-18102A>C	XP_011534263.1:n.703-18102A>C
XM_011535961.3:c.703-18102A>C	XP_011534263.1:n.703-18102A>C
XM_011535962.1:c.468+153A>C	XP_011534264.1:n.468+153A>C
XM_011535962.2:c.468+153A>C	XP_011534264.1:n.468+153A>C
XM_017011082.2:c.876+153A>C	XP_016866571.1:n.876+153A>C