Canonical Allele Identifier: CA1323931462

Gene: CRYGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129618G= , CM000664.2:g.208129618G=	GRCh38
NC_000002.11:g.208994342G= , CM000664.1:g.208994342G=	GRCh37
NC_000002.10:g.208702587G=	NCBI36
NG_008038.1:g.5213C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282141.4:c.75C= MANE Select	ENSP00000282141.3:p.Asn25=
ENST00000282141.3:c.75C=	ENSP00000282141.3:p.Asn25=
NM_020989.3:c.75C=	NP_066269.1:p.Asn25=
NR_038437.1:n.98-7438G=
XM_011510661.1:c.75C=	XP_011508963.1:p.Asn25=
XM_011510662.1:c.75C=	XP_011508964.1:p.Asn25=
XM_011510663.1:c.-55C=	XP_011508965.1:n.-55C=
NM_020989.4:c.75C= MANE Select	NP_066269.1:p.Asn25=