Canonical Allele Identifier: CA645517837

Gene: ALB

Linked Data

• COSMIC: COSM217317

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408783_73408784del , CM000666.2:g.73408783_73408784del	GRCh38
NC_000004.11:g.74274500_74274501del , CM000666.1:g.74274500_74274501del	GRCh37
NC_000004.10:g.74493364_74493365del	NCBI36
NG_009291.1:g.9529_9530del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.460_461del MANE Select	ENSP00000295897.4:p.Asn154Ter
ENST00000295897.8:c.460_461del	ENSP00000295897.4:p.Asn154Ter
ENST00000401494.7:c.138-572_138-571del	ENSP00000384695.3:n.138-572_138-571del
ENST00000415165.6:c.138-3213_138-3212del	ENSP00000401820.2:n.138-3213_138-3212del
ENST00000441319.5:c.466_467del	ENSP00000392541.1:p.Asn156Ter
ENST00000476441.6:c.80-572_80-571del	ENSP00000423727.1:n.80-572_80-571del
ENST00000503124.5:c.33-572_33-571del	ENSP00000421027.1:n.33-572_33-571del
ENST00000505649.5:n.146_147del
ENST00000509063.5:c.460_461del	ENSP00000422784.1:p.Asn154Ter
ENST00000510166.5:n.496_497del
ENST00000514786.1:n.429_430del
ENST00000515133.5:n.501_502del
ENST00000621085.4:c.460_461del	ENSP00000483421.1:p.Asn154Ter
ENST00000621628.4:c.460_461del	ENSP00000480485.1:p.Asn154Ter
NM_000477.5:c.460_461del	NP_000468.1:p.Asn154Ter
NM_000477.6:c.460_461del	NP_000468.1:p.Asn154Ter
NM_000477.7:c.460_461del MANE Select	NP_000468.1:p.Asn154Ter