Canonical Allele Identifier: CA1335698062

Gene: SAG

Linked Data

• dbSNP Id: rs1701264433

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346772_233346777del , CM000664.2:g.233346772_233346777del	GRCh38
NC_000002.11:g.234255418_234255423del , CM000664.1:g.234255418_234255423del	GRCh37
NC_000002.10:g.233920157_233920162del	NCBI36
NG_009116.1:g.44110_44115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1113-35_1113-30del MANE Select	ENSP00000386444.1:n.1113-35_1113-30del
ENST00000409110.5:c.1113-35_1113-30del	ENSP00000386444.1:n.1113-35_1113-30del
ENST00000412969.6:n.2333-35_2333-30del
ENST00000471884.5:n.3144-35_3144-30del
ENST00000474220.5:n.319-35_319-30del
ENST00000476500.5:n.6412-35_6412-30del
ENST00000492629.1:n.74-35_74-30del
NM_000541.4:c.1113-35_1113-30del	NP_000532.2:n.1113-35_1113-30del
XM_011511589.1:c.1113-35_1113-30del	XP_011509891.1:n.1113-35_1113-30del
XM_011511590.1:c.1113-35_1113-30del	XP_011509892.1:n.1113-35_1113-30del
XM_011511591.1:c.1103-35_1103-30del	XP_011509893.1:n.1103-35_1103-30del
XM_011511592.1:c.957-35_957-30del	XP_011509894.1:n.957-35_957-30del
XM_011511593.1:c.813-35_813-30del	XP_011509895.1:n.813-35_813-30del
XM_011511594.1:c.741-35_741-30del	XP_011509896.1:n.741-35_741-30del
XM_011511596.1:c.711-35_711-30del	XP_011509898.1:n.711-35_711-30del
XM_011511597.1:c.711-35_711-30del	XP_011509899.1:n.711-35_711-30del
XR_922978.1:n.1430-35_1430-30del
XR_922979.1:n.1434-35_1434-30del
XR_922980.1:n.1529-35_1529-30del
XM_011511593.3:c.813-35_813-30del	XP_011509895.1:n.813-35_813-30del
XM_017004641.1:c.1103-35_1103-30del	XP_016860130.1:n.1103-35_1103-30del
XM_024453036.1:c.701-35_701-30del	XP_024308804.1:n.701-35_701-30del
XR_001738882.1:n.1311-35_1311-30del
XR_922980.2:n.1529-35_1529-30del
NM_000541.5:c.1113-35_1113-30del MANE Select	NP_000532.2:n.1113-35_1113-30del