Canonical Allele Identifier: CA2670936992

Gene: ALB

Linked Data

• gnomAD v4: 4-73408753-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408755del , CM000666.2:g.73408755del	GRCh38
NC_000004.11:g.74274472del , CM000666.1:g.74274472del	GRCh37
NC_000004.10:g.74493336del	NCBI36
NG_009291.1:g.9501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.432del MANE Select	ENSP00000295897.4:p.Asp145MetfsTer2
ENST00000295897.8:c.432del	ENSP00000295897.4:p.Asp145MetfsTer2
ENST00000401494.7:c.138-600del	ENSP00000384695.3:n.138-600del
ENST00000415165.6:c.138-3241del	ENSP00000401820.2:n.138-3241del
ENST00000441319.5:c.438del	ENSP00000392541.1:p.Asp147MetfsTer2
ENST00000476441.6:c.80-600del	ENSP00000423727.1:n.80-600del
ENST00000503124.5:c.33-600del	ENSP00000421027.1:n.33-600del
ENST00000505649.5:n.118del
ENST00000509063.5:c.432del	ENSP00000422784.1:p.Asp145MetfsTer2
ENST00000510166.5:n.468del
ENST00000514786.1:n.401del
ENST00000515133.5:n.473del
ENST00000621085.4:c.432del	ENSP00000483421.1:p.Asp145MetfsTer2
ENST00000621628.4:c.432del	ENSP00000480485.1:p.Asp145MetfsTer2
NM_000477.5:c.432del	NP_000468.1:p.Asp145MetfsTer2
NM_000477.6:c.432del	NP_000468.1:p.Asp145MetfsTer2
NM_000477.7:c.432del MANE Select	NP_000468.1:p.Asp145MetfsTer2