Canonical Allele Identifier: CA2663686013

Gene: SAG

Linked Data

• gnomAD v4: 2-233346779-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346779G>C , CM000664.2:g.233346779G>C	GRCh38
NC_000002.11:g.234255425G>C , CM000664.1:g.234255425G>C	GRCh37
NC_000002.10:g.233920164G>C	NCBI36
NG_009116.1:g.44117G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1113-28G>C MANE Select	ENSP00000386444.1:n.1113-28G>C
ENST00000409110.5:c.1113-28G>C	ENSP00000386444.1:n.1113-28G>C
ENST00000412969.6:n.2333-28G>C
ENST00000471884.5:n.3144-28G>C
ENST00000474220.5:n.319-28G>C
ENST00000476500.5:n.6412-28G>C
ENST00000492629.1:n.74-28G>C
NM_000541.4:c.1113-28G>C	NP_000532.2:n.1113-28G>C
XM_011511589.1:c.1113-28G>C	XP_011509891.1:n.1113-28G>C
XM_011511590.1:c.1113-28G>C	XP_011509892.1:n.1113-28G>C
XM_011511591.1:c.1103-28G>C	XP_011509893.1:n.1103-28G>C
XM_011511592.1:c.957-28G>C	XP_011509894.1:n.957-28G>C
XM_011511593.1:c.813-28G>C	XP_011509895.1:n.813-28G>C
XM_011511594.1:c.741-28G>C	XP_011509896.1:n.741-28G>C
XM_011511596.1:c.711-28G>C	XP_011509898.1:n.711-28G>C
XM_011511597.1:c.711-28G>C	XP_011509899.1:n.711-28G>C
XR_922978.1:n.1430-28G>C
XR_922979.1:n.1434-28G>C
XR_922980.1:n.1529-28G>C
XM_011511593.3:c.813-28G>C	XP_011509895.1:n.813-28G>C
XM_017004641.1:c.1103-28G>C	XP_016860130.1:n.1103-28G>C
XM_024453036.1:c.701-28G>C	XP_024308804.1:n.701-28G>C
XR_001738882.1:n.1311-28G>C
XR_922980.2:n.1529-28G>C
NM_000541.5:c.1113-28G>C MANE Select	NP_000532.2:n.1113-28G>C