Canonical Allele Identifier: CA490206351

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003335A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711137A>G , CM000677.2:g.44711137A>G	GRCh38
NC_000015.9:g.45003335A>G , CM000677.1:g.45003335A>G	GRCh37
NC_000015.8:g.42790627A>G	NCBI36
NG_012920.1:g.4651A>G
NG_012920.2:g.4661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-371T>C MANE Select	ENSP00000508024.1:n.-371T>C
ENST00000558573.1:n.180T>C
XM_011521338.1:c.-371T>C	XP_011519640.1:n.-371T>C
XM_011521339.1:c.-252T>C	XP_011519641.1:n.-252T>C
XM_011521340.1:c.-193T>C	XP_011519642.1:n.-193T>C
XM_011521343.1:c.-455T>C	XP_011519645.1:n.-455T>C
XM_011521345.1:c.-426T>C	XP_011519647.1:n.-426T>C
XM_011521338.3:c.-371T>C	XP_011519640.1:n.-371T>C
XM_011521339.3:c.-252T>C	XP_011519641.1:n.-252T>C
XM_011521340.3:c.-193T>C	XP_011519642.1:n.-193T>C
XM_011521343.3:c.-455T>C	XP_011519645.1:n.-455T>C
XM_011521345.3:c.-426T>C	XP_011519647.1:n.-426T>C
NM_001387260.1:c.-76+195T>C	NP_001374189.1:n.-76+195T>C
NM_001387261.1:c.-193T>C	NP_001374190.1:n.-193T>C
NM_001387262.1:c.-461T>C	NP_001374191.1:n.-461T>C
NM_001387263.1:c.-371T>C MANE Select	NP_001374192.1:n.-371T>C