Canonical Allele Identifier: CA99701110

Gene: ALB

Linked Data

• dbSNP Id: rs397935206
• MyVariant Identifiers: chr4:g.74274889_74274890insACAT (hg19) ; chr4:g.73409172_73409173insACAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409172_73409173insACAT , CM000666.2:g.73409172_73409173insACAT	GRCh38
NC_000004.11:g.74274889_74274890insACAT , CM000666.1:g.74274889_74274890insACAT	GRCh37
NC_000004.10:g.74493753_74493754insACAT	NCBI36
NG_009291.1:g.9918_9919insACAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.483-183_483-182insACAT MANE Select	ENSP00000295897.4:n.483-183_483-182insACAT
ENST00000295897.8:c.483-183_483-182insACAT	ENSP00000295897.4:n.483-183_483-182insACAT
ENST00000401494.7:c.138-183_138-182insACAT	ENSP00000384695.3:n.138-183_138-182insACAT
ENST00000415165.6:c.138-2824_138-2823insACAT	ENSP00000401820.2:n.138-2824_138-2823insACAT
ENST00000441319.5:c.489-183_489-182insACAT	ENSP00000392541.1:n.489-183_489-182insACAT
ENST00000476441.6:c.80-183_80-182insACAT	ENSP00000423727.1:n.80-183_80-182insACAT
ENST00000503124.5:c.33-183_33-182insACAT	ENSP00000421027.1:n.33-183_33-182insACAT
ENST00000505649.5:n.169-183_169-182insACAT
ENST00000509063.5:c.483-183_483-182insACAT	ENSP00000422784.1:n.483-183_483-182insACAT
ENST00000514786.1:n.452-183_452-182insACAT
ENST00000621085.4:c.483-183_483-182insACAT	ENSP00000483421.1:n.483-183_483-182insACAT
ENST00000621628.4:c.486+96_486+97insACAT	ENSP00000480485.1:n.486+96_486+97insACAT
NM_000477.5:c.483-183_483-182insACAT	NP_000468.1:n.483-183_483-182insACAT
NM_000477.6:c.483-183_483-182insACAT	NP_000468.1:n.483-183_483-182insACAT
NM_000477.7:c.483-183_483-182insACAT MANE Select	NP_000468.1:n.483-183_483-182insACAT