Canonical Allele Identifier: CA490206642

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003429A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711231A>C , CM000677.2:g.44711231A>C	GRCh38
NC_000015.9:g.45003429A>C , CM000677.1:g.45003429A>C	GRCh37
NC_000015.8:g.42790721A>C	NCBI36
NG_012920.1:g.4745A>C
NG_012920.2:g.4755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-465T>G MANE Select	ENSP00000508024.1:n.-465T>G
ENST00000558573.1:n.86T>G
XM_011521338.1:c.-465T>G	XP_011519640.1:n.-465T>G
XM_011521339.1:c.-346T>G	XP_011519641.1:n.-346T>G
XM_011521340.1:c.-287T>G	XP_011519642.1:n.-287T>G
XM_011521343.1:c.-549T>G	XP_011519645.1:n.-549T>G
XM_011521345.1:c.-520T>G	XP_011519647.1:n.-520T>G
XM_011521338.3:c.-465T>G	XP_011519640.1:n.-465T>G
XM_011521339.3:c.-346T>G	XP_011519641.1:n.-346T>G
XM_011521340.3:c.-287T>G	XP_011519642.1:n.-287T>G
XM_011521343.3:c.-549T>G	XP_011519645.1:n.-549T>G
XM_011521345.3:c.-520T>G	XP_011519647.1:n.-520T>G
NM_001387260.1:c.-76+101T>G	NP_001374189.1:n.-76+101T>G
NM_001387261.1:c.-287T>G	NP_001374190.1:n.-287T>G
NM_001387262.1:c.-555T>G	NP_001374191.1:n.-555T>G
NM_001387263.1:c.-465T>G MANE Select	NP_001374192.1:n.-465T>G