Canonical Allele Identifier: CA490206656

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711236-G-A
• MyVariant Identifiers: chr15:g.45003434G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711236G>A , CM000677.2:g.44711236G>A	GRCh38
NC_000015.9:g.45003434G>A , CM000677.1:g.45003434G>A	GRCh37
NC_000015.8:g.42790726G>A	NCBI36
NG_012920.1:g.4750G>A
NG_012920.2:g.4760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-470C>T MANE Select	ENSP00000508024.1:n.-470C>T
ENST00000558573.1:n.81C>T
XM_011521338.1:c.-470C>T	XP_011519640.1:n.-470C>T
XM_011521339.1:c.-351C>T	XP_011519641.1:n.-351C>T
XM_011521340.1:c.-292C>T	XP_011519642.1:n.-292C>T
XM_011521343.1:c.-554C>T	XP_011519645.1:n.-554C>T
XM_011521345.1:c.-525C>T	XP_011519647.1:n.-525C>T
XM_011521338.3:c.-470C>T	XP_011519640.1:n.-470C>T
XM_011521339.3:c.-351C>T	XP_011519641.1:n.-351C>T
XM_011521340.3:c.-292C>T	XP_011519642.1:n.-292C>T
XM_011521343.3:c.-554C>T	XP_011519645.1:n.-554C>T
XM_011521345.3:c.-525C>T	XP_011519647.1:n.-525C>T
NM_001387260.1:c.-76+96C>T	NP_001374189.1:n.-76+96C>T
NM_001387261.1:c.-292C>T	NP_001374190.1:n.-292C>T
NM_001387262.1:c.-560C>T	NP_001374191.1:n.-560C>T
NM_001387263.1:c.-470C>T MANE Select	NP_001374192.1:n.-470C>T