Canonical Allele Identifier: CA2620277330

Gene: HAL

Linked Data

• gnomAD v4: 12-95980747-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95980747G>A , CM000674.2:g.95980747G>A	GRCh38
NC_000012.11:g.96374525G>A , CM000674.1:g.96374525G>A	GRCh37
NC_000012.10:g.94898656G>A	NCBI36
NG_008180.1:g.20547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.1354-26C>T MANE Select	ENSP00000261208.3:n.1354-26C>T
ENST00000261208.7:c.1354-26C>T	ENSP00000261208.3:n.1354-26C>T
ENST00000538703.5:c.1354-26C>T	ENSP00000440861.1:n.1354-26C>T
ENST00000541929.5:c.730-26C>T	ENSP00000446364.1:n.730-26C>T
ENST00000544080.6:c.*783-26C>T	ENSP00000439385.2:n.*783-26C>T
ENST00000546999.5:c.*766-26C>T	ENSP00000447675.1:n.*766-26C>T
NM_001258333.1:c.730-26C>T	NP_001245262.1:n.730-26C>T
NM_001258334.1:c.1354-26C>T	NP_001245263.1:n.1354-26C>T
NM_002108.3:c.1354-26C>T	NP_002099.1:n.1354-26C>T
XM_011538249.1:c.502-26C>T	XP_011536551.1:n.502-26C>T
XM_011538249.2:c.502-26C>T	XP_011536551.1:n.502-26C>T
XM_017019246.1:c.424-26C>T	XP_016874735.1:n.424-26C>T
NM_002108.4:c.1354-26C>T MANE Select	NP_002099.1:n.1354-26C>T
NM_001258334.2:c.1354-26C>T	NP_001245263.1:n.1354-26C>T
NM_001258333.2:c.730-26C>T	NP_001245262.1:n.730-26C>T