Canonical Allele Identifier: CA490206393

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711150-C-A
• MyVariant Identifiers: chr15:g.45003348C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711150C>A , CM000677.2:g.44711150C>A	GRCh38
NC_000015.9:g.45003348C>A , CM000677.1:g.45003348C>A	GRCh37
NC_000015.8:g.42790640C>A	NCBI36
NG_012920.1:g.4664C>A
NG_012920.2:g.4674C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-384G>T MANE Select	ENSP00000508024.1:n.-384G>T
ENST00000558573.1:n.167G>T
XM_011521338.1:c.-384G>T	XP_011519640.1:n.-384G>T
XM_011521339.1:c.-265G>T	XP_011519641.1:n.-265G>T
XM_011521340.1:c.-206G>T	XP_011519642.1:n.-206G>T
XM_011521343.1:c.-468G>T	XP_011519645.1:n.-468G>T
XM_011521345.1:c.-439G>T	XP_011519647.1:n.-439G>T
XM_011521338.3:c.-384G>T	XP_011519640.1:n.-384G>T
XM_011521339.3:c.-265G>T	XP_011519641.1:n.-265G>T
XM_011521340.3:c.-206G>T	XP_011519642.1:n.-206G>T
XM_011521343.3:c.-468G>T	XP_011519645.1:n.-468G>T
XM_011521345.3:c.-439G>T	XP_011519647.1:n.-439G>T
NM_001387260.1:c.-76+182G>T	NP_001374189.1:n.-76+182G>T
NM_001387261.1:c.-206G>T	NP_001374190.1:n.-206G>T
NM_001387262.1:c.-474G>T	NP_001374191.1:n.-474G>T
NM_001387263.1:c.-384G>T MANE Select	NP_001374192.1:n.-384G>T