Canonical Allele Identifier: CA1468141820

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413284_73413286delinsCAG , CM000666.2:g.73413284_73413286delinsCAG	GRCh38
NC_000004.11:g.74279001_74279003delinsCAG , CM000666.1:g.74279001_74279003delinsCAG	GRCh37
NC_000004.10:g.74497865_74497867delinsCAG	NCBI36
NG_009291.1:g.14030_14032delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-136_844-134delinsCAG MANE Select	ENSP00000295897.4:n.844-136_844-134delinsCAG
ENST00000295897.8:c.844-136_844-134delinsCAG	ENSP00000295897.4:n.844-136_844-134delinsCAG
ENST00000401494.7:c.499-136_499-134delinsCAG	ENSP00000384695.3:n.499-136_499-134delinsCAG
ENST00000415165.6:c.268-136_268-134delinsCAG	ENSP00000401820.2:n.268-136_268-134delinsCAG
ENST00000476441.6:c.*123-136_*123-134delinsCAG	ENSP00000423727.1:n.*123-136_*123-134delinsCAG
ENST00000484992.1:n.28_30delinsCAG
ENST00000503124.5:c.394-136_394-134delinsCAG	ENSP00000421027.1:n.394-136_394-134delinsCAG
ENST00000505649.5:n.530-136_530-134delinsCAG
ENST00000509063.5:c.844-136_844-134delinsCAG	ENSP00000422784.1:n.844-136_844-134delinsCAG
ENST00000511370.1:c.377-136_377-134delinsCAG
ENST00000621085.4:c.491-1822_491-1820delinsCAG	ENSP00000483421.1:n.491-1822_491-1820delinsCAG
ENST00000621628.4:c.487-1818_487-1816delinsCAG	ENSP00000480485.1:n.487-1818_487-1816delinsCAG
NM_000477.5:c.844-136_844-134delinsCAG	NP_000468.1:n.844-136_844-134delinsCAG
NM_000477.6:c.844-136_844-134delinsCAG	NP_000468.1:n.844-136_844-134delinsCAG
NM_000477.7:c.844-136_844-134delinsCAG MANE Select	NP_000468.1:n.844-136_844-134delinsCAG