Canonical Allele Identifier: CA385825561

Gene: CSRP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.76863215T>G , CM000674.2:g.76863215T>G	GRCh38
NC_000012.11:g.77256995T>G , CM000674.1:g.77256995T>G	GRCh37
NC_000012.10:g.75781126T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001321.3:c.242A>C MANE Select	NP_001312.1:p.Asn81Thr
ENST00000311083.10:c.242A>C MANE Select	ENSP00000310901.5:p.Asn81Thr
NM_001300965.1:c.242A>C	NP_001287894.1:p.Asn81Thr
NM_001300965.2:c.242A>C	NP_001287894.1:p.Asn81Thr
NM_001321.2:c.242A>C	NP_001312.1:p.Asn81Thr
ENST00000311083.9:c.242A>C	ENSP00000310901.5:p.Asn81Thr
ENST00000546966.5:c.242A>C	ENSP00000450056.1:p.Asn81Thr
ENST00000547435.1:c.242A>C	ENSP00000450143.1:p.Asn81Thr
ENST00000548783.1:n.1740A>C
ENST00000552330.5:c.242A>C	ENSP00000449824.1:p.Asn81Thr
XM_011537977.1:c.242A>C	XP_011536279.1:p.Asn81Thr