Canonical Allele Identifier: CA490206004

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711048-T-C
• MyVariant Identifiers: chr15:g.45003246T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711048T>C , CM000677.2:g.44711048T>C	GRCh38
NC_000015.9:g.45003246T>C , CM000677.1:g.45003246T>C	GRCh37
NC_000015.8:g.42790538T>C	NCBI36
NG_012920.1:g.4562T>C
NG_012920.2:g.4572T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-282A>G MANE Select	ENSP00000508024.1:n.-282A>G
ENST00000558573.1:n.269A>G
XM_011521338.1:c.-282A>G	XP_011519640.1:n.-282A>G
XM_011521339.1:c.-163A>G	XP_011519641.1:n.-163A>G
XM_011521340.1:c.-104A>G	XP_011519642.1:n.-104A>G
XM_011521343.1:c.-366A>G	XP_011519645.1:n.-366A>G
XM_011521345.1:c.-337A>G	XP_011519647.1:n.-337A>G
XM_011521338.3:c.-282A>G	XP_011519640.1:n.-282A>G
XM_011521339.3:c.-163A>G	XP_011519641.1:n.-163A>G
XM_011521340.3:c.-104A>G	XP_011519642.1:n.-104A>G
XM_011521343.3:c.-366A>G	XP_011519645.1:n.-366A>G
XM_011521345.3:c.-337A>G	XP_011519647.1:n.-337A>G
NM_001387260.1:c.-76+284A>G	NP_001374189.1:n.-76+284A>G
NM_001387261.1:c.-104A>G	NP_001374190.1:n.-104A>G
NM_001387262.1:c.-372A>G	NP_001374191.1:n.-372A>G
NM_001387263.1:c.-282A>G MANE Select	NP_001374192.1:n.-282A>G