Canonical Allele Identifier: CA2628214283

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711209-TGCAAAGCGAGGGGGCAGCCTTAATGTGCCTCCAGCCTGAAGTCCTAGAATGAGCGCCCGGTGTCCCAAGCTGGGGCGCGCACCCCAGATCGGAGGGCGCCGATGTACAGACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711215_44711326del , CM000677.2:g.44711215_44711326del	GRCh38
NC_000015.9:g.45003413_45003524del , CM000677.1:g.45003413_45003524del	GRCh37
NC_000015.8:g.42790705_42790816del	NCBI36
NG_012920.1:g.4729_4840del
NG_012920.2:g.4739_4850del

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-555_-444del	XP_011519640.1:n.-555_-444del
XM_011521339.1:c.-436_-325del	XP_011519641.1:n.-436_-325del
XM_011521340.1:c.-377_-266del	XP_011519642.1:n.-377_-266del
XM_011521343.1:c.-639_-528del	XP_011519645.1:n.-639_-528del
XM_011521345.1:c.-610_-499del	XP_011519647.1:n.-610_-499del
XM_011521338.3:c.-555_-444del	XP_011519640.1:n.-555_-444del
XM_011521339.3:c.-436_-325del	XP_011519641.1:n.-436_-325del
XM_011521340.3:c.-377_-266del	XP_011519642.1:n.-377_-266del
XM_011521343.3:c.-639_-528del	XP_011519645.1:n.-639_-528del
XM_011521345.3:c.-610_-499del	XP_011519647.1:n.-610_-499del
NM_001387260.1:c.-76+11_-76+122del	NP_001374189.1:n.-76+11_-76+122del