Canonical Allele Identifier: CA490206705

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003449T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711251T>G , CM000677.2:g.44711251T>G	GRCh38
NC_000015.9:g.45003449T>G , CM000677.1:g.45003449T>G	GRCh37
NC_000015.8:g.42790741T>G	NCBI36
NG_012920.1:g.4765T>G
NG_012920.2:g.4775T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-485A>C MANE Select	ENSP00000508024.1:n.-485A>C
ENST00000558573.1:n.66A>C
XM_011521338.1:c.-485A>C	XP_011519640.1:n.-485A>C
XM_011521339.1:c.-366A>C	XP_011519641.1:n.-366A>C
XM_011521340.1:c.-307A>C	XP_011519642.1:n.-307A>C
XM_011521343.1:c.-569A>C	XP_011519645.1:n.-569A>C
XM_011521345.1:c.-540A>C	XP_011519647.1:n.-540A>C
XM_011521338.3:c.-485A>C	XP_011519640.1:n.-485A>C
XM_011521339.3:c.-366A>C	XP_011519641.1:n.-366A>C
XM_011521340.3:c.-307A>C	XP_011519642.1:n.-307A>C
XM_011521343.3:c.-569A>C	XP_011519645.1:n.-569A>C
XM_011521345.3:c.-540A>C	XP_011519647.1:n.-540A>C
NM_001387260.1:c.-76+81A>C	NP_001374189.1:n.-76+81A>C
NM_001387261.1:c.-307A>C	NP_001374190.1:n.-307A>C
NM_001387262.1:c.-575A>C	NP_001374191.1:n.-575A>C
NM_001387263.1:c.-485A>C MANE Select	NP_001374192.1:n.-485A>C