Canonical Allele Identifier: CA490206825

Gene: PATL2

Linked Data

• dbSNP Id: rs1355834271
• MyVariant Identifiers: chr15:g.45003491C>T (hg19) ; chr15:g.44711293C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711293C>T , CM000677.2:g.44711293C>T	GRCh38
NC_000015.9:g.45003491C>T , CM000677.1:g.45003491C>T	GRCh37
NC_000015.8:g.42790783C>T	NCBI36
NG_012920.1:g.4807C>T
NG_012920.2:g.4817C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-527G>A MANE Select	ENSP00000508024.1:n.-527G>A
ENST00000558573.1:n.24G>A
XM_011521338.1:c.-527G>A	XP_011519640.1:n.-527G>A
XM_011521339.1:c.-408G>A	XP_011519641.1:n.-408G>A
XM_011521340.1:c.-349G>A	XP_011519642.1:n.-349G>A
XM_011521343.1:c.-611G>A	XP_011519645.1:n.-611G>A
XM_011521345.1:c.-582G>A	XP_011519647.1:n.-582G>A
XM_011521338.3:c.-527G>A	XP_011519640.1:n.-527G>A
XM_011521339.3:c.-408G>A	XP_011519641.1:n.-408G>A
XM_011521340.3:c.-349G>A	XP_011519642.1:n.-349G>A
XM_011521343.3:c.-611G>A	XP_011519645.1:n.-611G>A
XM_011521345.3:c.-582G>A	XP_011519647.1:n.-582G>A
NM_001387260.1:c.-76+39G>A	NP_001374189.1:n.-76+39G>A
NM_001387261.1:c.-349G>A	NP_001374190.1:n.-349G>A
NM_001387262.1:c.-617G>A	NP_001374191.1:n.-617G>A
NM_001387263.1:c.-527G>A MANE Select	NP_001374192.1:n.-527G>A