Canonical Allele Identifier: CA490206218

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003300G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711102G>T , CM000677.2:g.44711102G>T	GRCh38
NC_000015.9:g.45003300G>T , CM000677.1:g.45003300G>T	GRCh37
NC_000015.8:g.42790592G>T	NCBI36
NG_012920.1:g.4616G>T
NG_012920.2:g.4626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-336C>A MANE Select	ENSP00000508024.1:n.-336C>A
ENST00000558573.1:n.215C>A
XM_011521338.1:c.-336C>A	XP_011519640.1:n.-336C>A
XM_011521339.1:c.-217C>A	XP_011519641.1:n.-217C>A
XM_011521340.1:c.-158C>A	XP_011519642.1:n.-158C>A
XM_011521343.1:c.-420C>A	XP_011519645.1:n.-420C>A
XM_011521345.1:c.-391C>A	XP_011519647.1:n.-391C>A
XM_011521338.3:c.-336C>A	XP_011519640.1:n.-336C>A
XM_011521339.3:c.-217C>A	XP_011519641.1:n.-217C>A
XM_011521340.3:c.-158C>A	XP_011519642.1:n.-158C>A
XM_011521343.3:c.-420C>A	XP_011519645.1:n.-420C>A
XM_011521345.3:c.-391C>A	XP_011519647.1:n.-391C>A
NM_001387260.1:c.-76+230C>A	NP_001374189.1:n.-76+230C>A
NM_001387261.1:c.-158C>A	NP_001374190.1:n.-158C>A
NM_001387262.1:c.-426C>A	NP_001374191.1:n.-426C>A
NM_001387263.1:c.-336C>A MANE Select	NP_001374192.1:n.-336C>A