Canonical Allele Identifier: CA270113915

Gene: PATL2

Linked Data

• dbSNP Id: rs762218809
• gnomAD v3: 15-44711105-C-A
• gnomAD v4: 15-44711105-C-A
• MyVariant Identifiers: chr15:g.45003303C>A (hg19) ; chr15:g.44711105C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711105C>A , CM000677.2:g.44711105C>A	GRCh38
NC_000015.9:g.45003303C>A , CM000677.1:g.45003303C>A	GRCh37
NC_000015.8:g.42790595C>A	NCBI36
NG_012920.1:g.4619C>A
NG_012920.2:g.4629C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-339G>T MANE Select	ENSP00000508024.1:n.-339G>T
ENST00000558573.1:n.212G>T
XM_011521338.1:c.-339G>T	XP_011519640.1:n.-339G>T
XM_011521339.1:c.-220G>T	XP_011519641.1:n.-220G>T
XM_011521340.1:c.-161G>T	XP_011519642.1:n.-161G>T
XM_011521343.1:c.-423G>T	XP_011519645.1:n.-423G>T
XM_011521345.1:c.-394G>T	XP_011519647.1:n.-394G>T
XM_011521338.3:c.-339G>T	XP_011519640.1:n.-339G>T
XM_011521339.3:c.-220G>T	XP_011519641.1:n.-220G>T
XM_011521340.3:c.-161G>T	XP_011519642.1:n.-161G>T
XM_011521343.3:c.-423G>T	XP_011519645.1:n.-423G>T
XM_011521345.3:c.-394G>T	XP_011519647.1:n.-394G>T
NM_001387260.1:c.-76+227G>T	NP_001374189.1:n.-76+227G>T
NM_001387261.1:c.-161G>T	NP_001374190.1:n.-161G>T
NM_001387262.1:c.-429G>T	NP_001374191.1:n.-429G>T
NM_001387263.1:c.-339G>T MANE Select	NP_001374192.1:n.-339G>T