Canonical Allele Identifier: CA2670936469

Gene: ALB

Linked Data

• gnomAD v4: 4-73404355-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404360del , CM000666.2:g.73404360del	GRCh38
NC_000004.11:g.74270077del , CM000666.1:g.74270077del	GRCh37
NC_000004.10:g.74488941del	NCBI36
NG_009291.1:g.5106del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.33del MANE Select	ENSP00000295897.4:p.Leu12SerfsTer?
ENST00000295897.8:c.33del	ENSP00000295897.4:p.Leu12SerfsTer?
ENST00000401494.7:c.33del	ENSP00000384695.3:p.Leu12SerfsTer?
ENST00000415165.6:c.33del	ENSP00000401820.2:p.Leu12SerfsTer?
ENST00000441319.5:c.48-9del	ENSP00000392541.1:n.48-9del
ENST00000476441.6:c.33del	ENSP00000423727.1:p.Leu12SerfsTer19
ENST00000503124.5:c.-148del	ENSP00000421027.1:n.-148del
ENST00000509063.5:c.33del	ENSP00000422784.1:p.Leu12SerfsTer?
ENST00000510166.5:n.74del
ENST00000514786.1:n.48+24del
ENST00000515133.5:n.74del
ENST00000621085.4:c.33del	ENSP00000483421.1:p.Leu12SerfsTer?
ENST00000621628.4:c.33del	ENSP00000480485.1:p.Leu12SerfsTer?
NM_000477.5:c.33del	NP_000468.1:p.Leu12SerfsTer?
NM_000477.6:c.33del	NP_000468.1:p.Leu12SerfsTer?
NM_000477.7:c.33del MANE Select	NP_000468.1:p.Leu12SerfsTer?