Canonical Allele Identifier: CA2670936465

Gene: ALB

Linked Data

• gnomAD v4: 4-73404324-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404325del , CM000666.2:g.73404325del	GRCh38
NC_000004.11:g.74270042del , CM000666.1:g.74270042del	GRCh37
NC_000004.10:g.74488906del	NCBI36
NG_009291.1:g.5071del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.-3del MANE Select	ENSP00000295897.4:n.-3del
ENST00000295897.8:c.-3del	ENSP00000295897.4:n.-3del
ENST00000401494.7:c.-3del	ENSP00000384695.3:n.-3del
ENST00000415165.6:c.-3del	ENSP00000401820.2:n.-3del
ENST00000441319.5:c.48-44del	ENSP00000392541.1:n.48-44del
ENST00000476441.6:c.-3del	ENSP00000423727.1:n.-3del
ENST00000503124.5:c.-183del	ENSP00000421027.1:n.-183del
ENST00000509063.5:c.-3del	ENSP00000422784.1:n.-3del
ENST00000510166.5:n.39del
ENST00000514786.1:n.37del
ENST00000515133.5:n.39del
ENST00000621085.4:c.-3del	ENSP00000483421.1:n.-3del
ENST00000621628.4:c.-3del	ENSP00000480485.1:n.-3del
NM_000477.5:c.-3del	NP_000468.1:n.-3del
NM_000477.6:c.-3del	NP_000468.1:n.-3del
NM_000477.7:c.-3del MANE Select	NP_000468.1:n.-3del