Canonical Allele Identifier: CA127970

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73416262G>C , CM000666.2:g.73416262G>C	GRCh38
NC_000004.11:g.74281979G>C , CM000666.1:g.74281979G>C	GRCh37
NC_000004.10:g.74500843G>C	NCBI36
NG_009291.1:g.17008G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1198G>C MANE Select	ENSP00000295897.4:p.Glu400Gln
ENST00000295897.8:c.1198G>C	ENSP00000295897.4:p.Glu400Gln
ENST00000401494.7:c.853G>C	ENSP00000384695.3:p.Glu285Gln
ENST00000415165.6:c.622G>C	ENSP00000401820.2:p.Glu208Gln
ENST00000476441.6:c.*477G>C	ENSP00000423727.1:n.*477G>C
ENST00000484992.1:n.518G>C
ENST00000503124.5:c.748G>C	ENSP00000421027.1:p.Glu250Gln
ENST00000505649.5:n.884G>C
ENST00000509063.5:c.1198G>C	ENSP00000422784.1:p.Glu400Gln
ENST00000511370.1:c.731G>C
ENST00000621085.4:c.559G>C	ENSP00000483421.1:p.Glu187Gln
ENST00000621628.4:c.559G>C	ENSP00000480485.1:p.Glu187Gln
NM_000477.5:c.1198G>C	NP_000468.1:p.Glu400Gln
NM_000477.6:c.1198G>C	NP_000468.1:p.Glu400Gln
NM_000477.7:c.1198G>C MANE Select	NP_000468.1:p.Glu400Gln