Canonical Allele Identifier: CA2670937055

Gene: ALB

Linked Data

• gnomAD v4: 4-73408938-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408941del , CM000666.2:g.73408941del	GRCh38
NC_000004.11:g.74274658del , CM000666.1:g.74274658del	GRCh37
NC_000004.10:g.74493522del	NCBI36
NG_009291.1:g.9687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+136del MANE Select	ENSP00000295897.4:n.482+136del
ENST00000295897.8:c.482+136del	ENSP00000295897.4:n.482+136del
ENST00000401494.7:c.138-414del	ENSP00000384695.3:n.138-414del
ENST00000415165.6:c.138-3055del	ENSP00000401820.2:n.138-3055del
ENST00000441319.5:c.488+136del	ENSP00000392541.1:n.488+136del
ENST00000476441.6:c.80-414del	ENSP00000423727.1:n.80-414del
ENST00000503124.5:c.33-414del	ENSP00000421027.1:n.33-414del
ENST00000505649.5:n.168+136del
ENST00000509063.5:c.482+136del	ENSP00000422784.1:n.482+136del
ENST00000514786.1:n.451+136del
ENST00000515133.5:n.659del
ENST00000621085.4:c.482+136del	ENSP00000483421.1:n.482+136del
ENST00000621628.4:c.483-132del	ENSP00000480485.1:n.483-132del
NM_000477.5:c.482+136del	NP_000468.1:n.482+136del
NM_000477.6:c.482+136del	NP_000468.1:n.482+136del
NM_000477.7:c.482+136del MANE Select	NP_000468.1:n.482+136del