Canonical Allele Identifier: CA400601782
Gene: SMARCD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63837610G>A , CM000679.2:g.63837610G>A GRCh38
NC_000017.10:g.61914970G>A , CM000679.1:g.61914970G>A GRCh37
NC_000017.9:g.59268702G>A NCBI36
NG_053004.1:g.10382C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697953.1:n.120C>T
ENST00000698016.1:c.91C>T ENSP00000513502.1:p.Pro31Ser
ENST00000698022.1:c.49C>T ENSP00000513504.1:p.Pro17Ser
ENST00000698027.1:c.91C>T ENSP00000513505.1:p.Pro31Ser
ENST00000448276.7:c.232C>T MANE Select ENSP00000392617.2:p.Pro78Ser
ENST00000225742.13:c.7C>T ENSP00000225742.9:p.Pro3Ser
ENST00000323347.14:c.88C>T ENSP00000318451.10:p.Pro30Ser
ENST00000448276.6:c.232C>T ENSP00000392617.2:p.Pro78Ser
ENST00000577686.1:n.53-373C>T
ENST00000580054.1:c.16C>T ENSP00000463793.1:p.Pro6Ser
ENST00000584400.5:c.217-373C>T ENSP00000464503.1:n.217-373C>T
ENST00000613943.4:c.121C>T ENSP00000483605.1:p.Pro41Ser
NM_001098426.1:c.232C>T NP_001091896.1:p.Pro78Ser
XM_005257604.2:c.7C>T XP_005257661.2:p.Pro3Ser
NM_001330439.1:c.7C>T NP_001317368.1:p.Pro3Ser
NM_001330440.1:c.88C>T NP_001317369.1:p.Pro30Ser
NM_001098426.2:c.232C>T MANE Select NP_001091896.1:p.Pro78Ser
NM_001330440.2:c.88C>T NP_001317369.1:p.Pro30Ser