Canonical Allele Identifier: CA2762164302

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408722_73408778del , CM000666.2:g.73408722_73408778del	GRCh38
NC_000004.11:g.74274439_74274495del , CM000666.1:g.74274439_74274495del	GRCh37
NC_000004.10:g.74493303_74493359del	NCBI36
NG_009291.1:g.9468_9524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.399_455del MANE Select	ENSP00000295897.4:p.Pro134_His152del
ENST00000295897.8:c.399_455del	ENSP00000295897.4:p.Pro134_His152del
ENST00000401494.7:c.138-633_138-577del	ENSP00000384695.3:n.138-633_138-577del
ENST00000415165.6:c.138-3274_138-3218del	ENSP00000401820.2:n.138-3274_138-3218del
ENST00000441319.5:c.405_461del	ENSP00000392541.1:p.Pro136_His154del
ENST00000476441.6:c.80-633_80-577del	ENSP00000423727.1:n.80-633_80-577del
ENST00000503124.5:c.33-633_33-577del	ENSP00000421027.1:n.33-633_33-577del
ENST00000505649.5:n.85_141del
ENST00000509063.5:c.399_455del	ENSP00000422784.1:p.Pro134_His152del
ENST00000510166.5:n.435_491del
ENST00000514786.1:n.368_424del
ENST00000515133.5:n.440_496del
ENST00000621085.4:c.399_455del	ENSP00000483421.1:p.Pro134_His152del
ENST00000621628.4:c.399_455del	ENSP00000480485.1:p.Pro134_His152del
NM_000477.5:c.399_455del	NP_000468.1:p.Pro134_His152del
NM_000477.6:c.399_455del	NP_000468.1:p.Pro134_His152del
NM_000477.7:c.399_455del MANE Select	NP_000468.1:p.Pro134_His152del