Canonical Allele Identifier: CA1802300

Gene: CHST10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100393489A>G , CM000664.2:g.100393489A>G	GRCh38
NC_000002.11:g.101009951A>G , CM000664.1:g.101009951A>G	GRCh37
NC_000002.10:g.100376383A>G	NCBI36
NG_028153.1:g.29180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264249.8:c.827T>C MANE Select	ENSP00000264249.3:p.Met276Thr
ENST00000264249.7:c.827T>C	ENSP00000264249.3:p.Met276Thr
ENST00000409701.5:c.827T>C	ENSP00000387309.1:p.Met276Thr
NM_004854.4:c.827T>C	NP_004845.1:p.Met276Thr
XM_011512207.1:c.827T>C	XP_011510509.1:p.Met276Thr
XM_011512208.1:c.827T>C	XP_011510510.1:p.Met276Thr
XM_011512209.1:c.827T>C	XP_011510511.1:p.Met276Thr
XM_011512210.1:c.827T>C	XP_011510512.1:p.Met276Thr
XM_011512211.1:c.827T>C	XP_011510513.1:p.Met276Thr
XM_011512212.1:c.827T>C	XP_011510514.1:p.Met276Thr
XM_011512207.2:c.827T>C	XP_011510509.1:p.Met276Thr
XM_017005380.2:c.827T>C	XP_016860869.1:p.Met276Thr
XM_017005381.2:c.827T>C	XP_016860870.1:p.Met276Thr
XM_017005382.2:c.827T>C	XP_016860871.1:p.Met276Thr
XM_017005383.2:c.827T>C	XP_016860872.1:p.Met276Thr
XM_024453248.1:c.827T>C	XP_024309016.1:p.Met276Thr
NM_004854.5:c.827T>C MANE Select	NP_004845.1:p.Met276Thr